FDA Class II · Drug · May 13, 2026
BD PurPrep recall — CareFusion 213, LLC
Lack of assurance of Sterility: potential product contamination
Company / brand: CareFusion 213 recalls
Official ID D-0518-2026 · Official record ↗
Latest recalls — page 33
Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 3,201–3,300, newest first.
FDA Class II · Drug · May 13, 2026
BD PurPrep recall — CareFusion 213, LLC
Lack of assurance of Sterility: potential product contamination
Company / brand: CareFusion 213 recalls
Official ID D-0517-2026 · Official record ↗
FDA Class II · Drug · May 13, 2026
Duloxetine Delayed-Release Capsules recall — Ajanta Pharma Ltd.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
Company / brand: Ajanta Pharma recalls
Official ID D-0516-2026 · Official record ↗
FDA Class II · Drug · May 13, 2026
Duloxetine Delayed-Release Capsules recall — Ajanta Pharma Ltd.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
Company / brand: Ajanta Pharma recalls
Official ID D-0515-2026 · Official record ↗
FDA Class II · Drug · May 13, 2026
Duloxetine Delayed-Release Capsules recall — Ajanta Pharma Ltd.
CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.
Company / brand: Ajanta Pharma recalls
Official ID D-0514-2026 · Official record ↗
FDA Class II · Drug · May 13, 2026
DELFLEX recall — Fresenius Medical Care Holdings, Inc.
Lack of Assurance of Sterility: Potential leaks from perforations in bags.
Company / brand: Fresenius Medical Care Holdings recalls
Official ID D-0513-2026 · Official record ↗
FDA Class II · Drug · May 13, 2026
DELFLEX recall — Fresenius Medical Care Holdings, Inc.
Lack of Assurance of Sterility: Potential leaks from perforations in bags.
Company / brand: Fresenius Medical Care Holdings recalls
Official ID D-0512-2026 · Official record ↗
FDA Class III · Drug · May 13, 2026
busPIRone Hydrochloride Tablets recall — Unichem Pharmaceuticals USA Inc.
Subpotent drug
Company / brand: Unichem Pharmaceuticals USA recalls
Official ID D-0511-2026 · Official record ↗
NHTSA · Vehicle · May 12, 2026
Piaggio Group Americas Visibility recall (26V302000)
Without the convex mirror warning, riders may misjudge the distance of other vehicles, resulting in unsafe lane changes or maneuvers, increasing the risk of a crash.
Company / brand: Piaggio Group Americas recalls
Official ID 26V302000 · Official record ↗
NHTSA · Vehicle · May 12, 2026
Ford Motor Company Power Train recall (26V301000)
A loss of park function can allow the vehicle to rollaway, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V301000 · Official record ↗
NHTSA · Vehicle · May 12, 2026
Nova Bus Structure recall (26V300000)
A missing DOT code mark may result in the door being replaced with the incorrect type of plastic, reducing visibility and increasing the risk of a crash.
Company / brand: Nova Bus recalls
Official ID 26V300000 · Official record ↗
NHTSA · Vehicle · May 12, 2026
Ford Bronco recall (26V299000)
A detached section of roof can create a road hazard, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V299000 · Official record ↗
NHTSA · Vehicle · May 12, 2026
Jaguar Land Rover North America Seat Belts recall (26V297000)
A seat belt chime that fails to alert occupants that they are unbuckled can increase the risk of injury during a crash.
Company / brand: Jaguar Land Rover North America recalls
Official ID 26V297000 · Official record ↗
NHTSA · Vehicle · May 11, 2026
Chrysler Pacifica recall (26V296000)
An unsecured wheelchair can move during transit, increasing the risk of injury.
Company / brand: Braun recalls
Official ID 26V296000 · Official record ↗
NHTSA · Vehicle · May 11, 2026
Prime Time Crusader recall (26V295000)
Sewer gas inside the vehicle may increase the risk of injury.
Company / brand: Forest River recalls
Official ID 26V295000 · Official record ↗
NHTSA · Vehicle · May 11, 2026
International HV recall (26V294000)
A delayed brake release can increase the risk of crash.
Company / brand: International Motors recalls
Official ID 26V294000 · Official record ↗
NHTSA · Vehicle equipment · May 11, 2026
Beck Arnley Lower Control Arm Assembly recall (26E028000)
A loose nut may allow the ball joint to separate from the control arm, causing a loss of steering control and increasing the risk of a crash.
Company / brand: Tenneco Automotive recalls
Official ID 26E028000 · Official record ↗
NHTSA · Vehicle · May 8, 2026
FLY Wing Snake 250 Efi recall (26V293000)
The braking performance in wet road conditions may be reduced, resulting in extended braking distance, increasing the risk of a crash.
Company / brand: Taizhou Qianxin Vehicle CO recalls
Official ID 26V293000 · Official record ↗
NHTSA · Vehicle · May 8, 2026
SHYFT Group Exterior Lighting recall (26V292000)
Brake lights that remain on may fail to alert other vehicles of the driver's intention, increasing the risk of a crash.
Company / brand: SHYFT Group recalls
Official ID 26V292000 · Official record ↗
NHTSA · Vehicle · May 8, 2026
Fontaine Fusion Flat Bed Trailer recall (26V291000)
A cracked beam may break, resulting in a loss of load support and increasing the risk of a crash or injury.
Company / brand: Fontaine Trailer Company recalls
Official ID 26V291000 · Official record ↗
NHTSA · Vehicle equipment · May 8, 2026
Dometic Fan-Tastic Vent Fan recall (26E027000)
A detached lid can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Dometic recalls
Official ID 26E027000 · Official record ↗
NHTSA · Vehicle · May 7, 2026
Jeep Cherokee recall (26V290000)
A failed PTU may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash or injury.
Company / brand: Chrysler recalls
Official ID 26V290000 · Official record ↗
NHTSA · Vehicle · May 7, 2026
General Motors Power Train recall (26V289000)
Front or rear wheel lockup increases the risk of a crash.
Company / brand: General Motors recalls
Official ID 26V289000 · Official record ↗
NHTSA · Vehicle · May 7, 2026
Ram 2500 recall (26V288000)
Loss of vehicle control increases the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V288000 · Official record ↗
CPSC · Consumer Product · May 7, 2026
EVLWZL and Gunugu Mattresses Recalled Due to Risk of Serious Injury or Death from Fire Hazard; Violates Mandatory Standard for Mattress Flammability
The mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.
Company / brand: Foshan Kangzhibao Furniture Co recalls
Official ID 26478 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
Allura Imports Recalls Youth Sweatshirts with Bobcat Logo and Drawstrings Due to Risk of Serious Injury or Death from Strangulation Hazard; Violates Federal Regulations for Children's Upper Outerwear
The drawstrings in the recalled clothing can get caught on objects and cause death or serious injury to children from strangulation. The sweatshirts are in violation of the federal…
Company / brand: Allura Imports recalls
Official ID 26477 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
Analemma Water Bottles Recalled Due to Risk of Serious Injury or Death from Laceration and Ingestion Hazards; Imported by New Earth Technologies d.o.o.
The recalled water bottle's inner glass liner can break, posing a risk of serious injury or death from laceration and ingestion hazards.
Company / brand: New Earth Technologies d.o.o recalls
Official ID 26475 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
Rainbow Wall Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Children's Toys; Sold on Amazon by Justforjoyful
The recalled toys violate the mandatory safety standard for children's toys because the drumstick that is attached to the xylophone component has a spherical end that can pose a ch…
Company / brand: Shenzhen Jijia Trading Co recalls
Official ID 26472 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
Multi-Purpose Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Temu by Foubeaka and Geniuss
The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and certification requirements. The h…
Company / brand: Shenzhenshilingkexunkeji Co recalls
Official ID 26470 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
Natural Pigments Recalls Rublev Colours Gum Turpentine and Mineral Spirits Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
The gum turpentine and mineral spirits contain turpentine and low-viscosity hydrocarbons, respectively, which must be in child-resistant packaging, as required by the Poison Preven…
Company / brand: Natural Pigments recalls
Official ID 26469 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
Svnntaa Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation Hazards; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by Eokeanon
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of th…
Company / brand: shenzhenkaiwendishangmaoyouxiangongsi (Shenzhen Kaiwendi Trading Co recalls
Official ID 26468 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
Favoto Bicycle Helmets Recalled Due to Risk of Serious Head Injury; Violate Mandatory Standard for Bicycle Helmets; Sold on Amazon by Favoto
The recalled helmets violate the mandatory safety standard for bicycle helmets because they do not comply with the positional stability, labeling and certification requirements. Th…
Company / brand: Shenzhen Favoto Co recalls
Official ID 26467 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
ZMC Group Recalls Multiple Light Up Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
The recalled toys violate the mandatory safety standard for children's toys because the toy contains button cell batteries that can be easily accessed by children. If button cell o…
Company / brand: ZMC Group recalls
Official ID 26466 · Official notice ↗
CPSC · Consumer Product · May 7, 2026
EEMB USA Recalls Battery Pouches Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Federal Statute for Child-Resistant Packaging of Coin Batteries
The lithium coin batteries are in pouches that are not child-resistant as required under Reese's Law. If a child swallows button cell or coin batteries, the ingested batteries can …
Company / brand: EEMB USA recalls
Official ID 26465 · Official notice ↗
NHTSA · Vehicle · May 6, 2026
Micro Bird Engine And Engine Cooling recall (26V287000)
A damaged oil like may leak, increasing the risk of a fire in the presence of an ignition source.
Company / brand: Micro Bird recalls
Official ID 26V287000 · Official record ↗
NHTSA · Vehicle · May 6, 2026
Micro Bird G5 Transit Bus recall (26V286000)
A damaged oil like may leak, increasing the risk of a fire in the presence of an ignition source.
Company / brand: Micro Bird recalls
Official ID 26V286000 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline and Centurion medical convenience kits recall — Medline Industries, LP
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Web…
Company / brand: Medline Industries recalls
Official ID Z-2045-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Centurion medical convenience kits recall — Medline Industries, LP
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Web…
Company / brand: Medline Industries recalls
Official ID Z-2044-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline or Centurion medical convenience kits recall — Medline Industries, LP
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Web…
Company / brand: Medline Industries recalls
Official ID Z-2043-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Centurion medical convenience kits recall — Medline Industries, LP
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Web…
Company / brand: Medline Industries recalls
Official ID Z-2042-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline and Centurion medical convenience kits recall — Medline Industries, LP
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Web…
Company / brand: Medline Industries recalls
Official ID Z-2041-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical convenience kits recall — Medline Industries, LP
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Web…
Company / brand: Medline Industries recalls
Official ID Z-2040-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Centurion medical convenience kits recall — Medline Industries, LP
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Web…
Company / brand: Medline Industries recalls
Official ID Z-2039-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2038-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2037-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2036-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2035-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2034-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2033-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2032-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2031-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2030-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2029-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Centurion medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2028-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2027-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2026-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2025-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2024-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2023-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2022-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline and Centurion medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2021-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2020-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2019-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2018-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2017-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2016-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2015-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2014-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2013-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2012-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2011-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2010-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline medical procedure kits recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2009-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Medline Neuro Sponges recall — Medline Industries, LP
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-o…
Company / brand: Medline Industries recalls
Official ID Z-2008-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Brand Name recall — Elekta, Inc.
Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.
Company / brand: Elekta recalls
Official ID Z-2006-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System recall — Siemens Healthcare Diagnostics Inc
Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial, venous, and capillary…
Company / brand: Siemens Healthcare Diagnostics recalls
Official ID Z-2005-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Philips Bridge Prep Kit REF recall — Merit Medical Systems, Inc.
catheter may experience resistance when being advanced over the guidewire
Company / brand: Merit Medical Systems recalls
Official ID Z-2004-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Philips Bridge Prep Kit REF recall — Merit Medical Systems, Inc.
catheter may experience resistance when being advanced over the guidewire
Company / brand: Merit Medical Systems recalls
Official ID Z-2003-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Philips Bridge Prep Kit REF recall — Merit Medical Systems, Inc.
catheter may experience resistance when being advanced over the guidewire
Company / brand: Merit Medical Systems recalls
Official ID Z-2002-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
i-STAT G3+ cartridge recall — Abbott Point Of Care Inc.
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.…
Company / brand: Abbott Point Of Care recalls
Official ID Z-2001-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
i-STAT EG6+ cartridge recall — Abbott Point Of Care Inc.
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.…
Company / brand: Abbott Point Of Care recalls
Official ID Z-2000-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
i-STAT EG7+ cartridge recall — Abbott Point Of Care Inc.
Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-25), i-STAT EG6+ (list number 03P77-25) and i-STAT G3+ (list number 03P78-26) cartridge lots in the U.…
Company / brand: Abbott Point Of Care recalls
Official ID Z-1999-2026 · Official record ↗
FDA Class III · Medical device · May 6, 2026
Heraeus recall — Heraeus Medical GmbH (Dental Division)
Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock during the mixing…
Company / brand: Heraeus Medical (Dental Division) recalls
Official ID Z-1998-2026 · Official record ↗
FDA Class III · Medical device · May 6, 2026
Heraeus recall — Heraeus Medical GmbH (Dental Division)
Based on long-term stability testing, it was determined that in units older than 1.5 years (17 months) the mixing rod may, in rare cases, come loose from its lock during the mixing…
Company / brand: Heraeus Medical (Dental Division) recalls
Official ID Z-1997-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
iLet Bionic Pancreas recall — Beta Bionics, Inc.
insulin pump software versions 1.4.2, and 1.4.3 issue with Dexcom Continuous Glucose Monitoring (CGM) G7 sensor may result in delayed CGM reading then switch to non-CGM dosing, lea…
Company / brand: Beta Bionics recalls
Official ID Z-1996-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Straumann n!ce Zr recall — Straumann USA LLC
Includes an incorrect screw seat interface.
Company / brand: Straumann USA recalls
Official ID Z-1995-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Straumann n!ce PMMA Full-arch Restoration recall — Straumann USA LLC
Includes an incorrect screw seat interface.
Company / brand: Straumann USA recalls
Official ID Z-1994-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1993-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1992-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1991-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1990-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1989-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1988-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1987-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1986-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Depuy Synthes recall — DEPUY (IRELAND)
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Company / brand: DEPUY (IRELAND) recalls
Official ID Z-1985-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Immy recall — Immuno-Mycologics, Inc
Neutralization Buffer may contain contaminants
Company / brand: Immuno-Mycologics recalls
Official ID Z-1984-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
BD GasPak EZ Campy Pouch System recall — Becton Dickinson & Co.
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide level…
Company / brand: Becton Dickinson & Co recalls
Official ID Z-1983-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
BD GasPak EZ CO2 Pouch System recall — Becton Dickinson & Co.
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide level…
Company / brand: Becton Dickinson & Co recalls
Official ID Z-1982-2026 · Official record ↗
FDA Class II · Medical device · May 6, 2026
Dimension Creatinine Flex reagent cartridge recall — Siemens Healthcare Diagnostics, Inc.
Siemens Healthcare Diagnostics is recalling certain lots of Dimension Creatinine Flex reagent cartridge (Dimension CRE2) because a potential imprecision in the Dimension CRE2 quali…
Company / brand: Siemens Healthcare Diagnostics recalls
Official ID Z-1980-2026 · Official record ↗
Official sources
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
Found something wrong or missing? Report a data error.
Government sources last checked October 22, 2026 at 12:00 PM UTC.