FDA Class II · Drug · October 7, 2026
FOCUS PI Hypromellose 0 recall — Aurolab Trust
Lack of Assurance of Sterility
Company / brand: Aurolab Trust recalls
Official ID D-0874-2026 · Official record ↗
Latest recalls — page 4
Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 301–400, newest first.
FDA Class II · Drug · October 7, 2026
Estradiol Gel recall — Amneal Pharmaceuticals, LLC
Defective Container; packets were found to be either empty or partially full.
Company / brand: Amneal Pharmaceuticals recalls
Official ID D-0873-2026 · Official record ↗
FDA Class II · Drug · October 7, 2026
Ranolazine Extended-Release Tablets recall — Ajanta Pharma USA Inc
Failed Dissolution Specifications: below specification
Company / brand: Ajanta Pharma USA recalls
Official ID D-0010-2027 · Official record ↗
NHTSA · Vehicle · October 6, 2026
Kovatch Mobile Equipment Equipment recall (26V657000)
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. A loss of pump-mode function may prevent or delay the use of em…
Company / brand: Kovatch Mobile Equipment recalls
Official ID 26V657000 · Official record ↗
NHTSA · Vehicle · October 6, 2026
Great Dane Champion recall (26V656000)
An improperly coupled trailer may detach, increasing the risk of a crash.
Company / brand: Great Dane Trailers recalls
Official ID 26V656000 · Official record ↗
NHTSA · Vehicle · October 6, 2026
Ford F-150 recall (26V655000)
An improperly secured seat may not adequately restrain the seat occupant, increasing the risk of injury during a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V655000 · Official record ↗
NHTSA · Vehicle · October 6, 2026
Spartan Fire Metrostar recall (26V654000)
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. A loss of pump-mode function may prevent or delay the use of em…
Company / brand: Spartan Fire recalls
Official ID 26V654000 · Official record ↗
NHTSA · Vehicle · October 6, 2026
Ford Motor Company Electrical System recall (26V653000)
A speedometer that fails to display accurate vehicle speed can increase the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V653000 · Official record ↗
NHTSA · Vehicle · October 6, 2026
E-One Incorporated Electrical System recall (26V652000)
An overheated busbar can increase the risk of a fire.
Company / brand: E-One Incorporated recalls
Official ID 26V652000 · Official record ↗
NHTSA · Vehicle · October 6, 2026
Ram 2500 recall (26V651000)
A loss of electronic stability control increases the risk of a crash.
Company / brand: Chrysler recalls
Official ID 26V651000 · Official record ↗
NHTSA · Vehicle · October 6, 2026
Ford Transit Connect recall (26V650000)
A rearview camera that displays an inverted, distorted, intermittent, or blank image can reduce the driver’s view behind the vehicle, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V650000 · Official record ↗
NHTSA · Vehicle · October 5, 2026
Rev Ambulance Group Orlando Equipment recall (26V649000)
A loss of warning lights can increase the risk of a crash.
Company / brand: Rev Ambulance Group Orlando recalls
Official ID 26V649000 · Official record ↗
NHTSA · Vehicle · October 5, 2026
Kalmar Ottawa T2 recall (26V648000)
A short circuit increases the risk of a fire even when the vehicle is parked and the ignition is in the 'Off' position.
Company / brand: Kalmar Solutions recalls
Official ID 26V648000 · Official record ↗
NHTSA · Vehicle · October 5, 2026
Forest River Surveyor recall (26V647000)
An outlet without GFCI protection may fail to shut off electrical power when a ground-fault occurs, increasing the risk of injury.
Company / brand: Forest River recalls
Official ID 26V647000 · Official record ↗
NHTSA · Vehicle · October 5, 2026
Forest River Equipment recall (26V646000)
A tire can be overinflated after referencing the incorrect information, increasing the risk of a crash.
Company / brand: Forest River recalls
Official ID 26V646000 · Official record ↗
NHTSA · Vehicle · October 5, 2026
Motor Coach Industries Electrical System recall (26V645000)
Without the illuminated reminder, the driver may fail to turn off the exterior lights when no longer needed. Hazard warning lights that remain activated unintentionally can confuse…
Company / brand: Motor Coach Industries recalls
Official ID 26V645000 · Official record ↗
NHTSA · Vehicle · October 5, 2026
New Flyer Exterior Lighting recall (26V644000)
Without the illuminated reminder, the driver may fail to turn off the exterior lights when no longer needed. Hazard warning lights that remain activated unintentionally can confuse…
Company / brand: New Flyer recalls
Official ID 26V644000 · Official record ↗
NHTSA · Vehicle · October 5, 2026
Greenpower Nano Beast School Bus recall (26V643000)
The bus moving while the wheelchair lift is in use increases the risk of injury.
Company / brand: Greenpower Motor Company recalls
Official ID 26V643000 · Official record ↗
NHTSA · Vehicle · October 2, 2026
Blue Bird All American Transit Bus (Electric) recall (26V642000)
A high voltage battery with loose or missing mounting bolts can cause a loss of drive power, increasing the risk of a crash.
Company / brand: Blue Bird Body Company recalls
Official ID 26V642000 · Official record ↗
NHTSA · Vehicle · October 2, 2026
Blue Bird Body Company Electrical System recall (26V641000)
A high voltage battery with loose or missing mounting bolts can cause a loss of drive power, increasing the risk of a crash.
Company / brand: Blue Bird Body Company recalls
Official ID 26V641000 · Official record ↗
NHTSA · Vehicle · October 2, 2026
Rosenbauer America Wheels recall (26V640000)
Wheel and/or tire failure increases the risk of a crash.
Company / brand: Rosenbauer America recalls
Official ID 26V640000 · Official record ↗
NHTSA · Vehicle · October 2, 2026
Ring Power Trailer Hitches recall (26V639000)
The pintle hitch may fail, causing a loss of trailer control and increasing the risk of a crash.
Company / brand: Ring Power recalls
Official ID 26V639000 · Official record ↗
NHTSA · Vehicle · October 2, 2026
Mercedes-Benz Usa Service Brakes, Hydraulic recall (26V638000)
A brake fluid leak can extend the distance needed to stop the vehicle, increasing the risk of a crash.
Company / brand: Mercedes-Benz Usa recalls
Official ID 26V638000 · Official record ↗
NHTSA · Vehicle · October 2, 2026
Altec Industries Structure recall (26V637000)
A step that separates or becomes unstable while in use, increases the risk of a fall or injury.
Company / brand: Altec Industries recalls
Official ID 26V637000 · Official record ↗
NHTSA · Vehicle · October 2, 2026
Mercedes-Benz Cla 220 recall (26V636000)
A seat belt with an incorrectly installed component may fail to properly restrain occupants, increasing the risk of injury during a crash.
Company / brand: Mercedes-Benz Usa recalls
Official ID 26V636000 · Official record ↗
NHTSA · Vehicle equipment · October 2, 2026
Roadmaster recall (26E069000)
A separated tow bar can result in the tow vehicle detaching, increases the risk of a crash.
Company / brand: Roadmaster recalls
Official ID 26E069000 · Official record ↗
NHTSA · Vehicle · October 1, 2026
Freightliner Business Class M2 recall (26V635000)
Insulation that comes into contact with hot exhaust components increases the risk of a fire.
Company / brand: Daimler Trucks North America recalls
Official ID 26V635000 · Official record ↗
NHTSA · Vehicle · October 1, 2026
Airstream recall (26V634000)
A detached fairing can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Airstream recalls
Official ID 26V634000 · Official record ↗
NHTSA · Vehicle · October 1, 2026
Honda Fuel System, Gasoline recall (26V633000)
Fuel pump failure can cause an engine stall, increasing the risk of a crash.
Company / brand: Honda recalls
Official ID 26V633000 · Official record ↗
NHTSA · Vehicle · October 1, 2026
Daimler Trucks North America Exterior Lighting recall (26V632000)
Insufficient low beam headlight illumination can reduce driver visibility, increasing the risk of a crash.
Company / brand: Daimler Trucks North America recalls
Official ID 26V632000 · Official record ↗
NHTSA · Vehicle · October 1, 2026
Mack Trucks Structure recall (26V631000)
A detached bezel can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Mack Trucks recalls
Official ID 26V631000 · Official record ↗
NHTSA · Vehicle equipment · October 1, 2026
Kuat Innovations recall (26E068000)
A detached cross beam can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Kuat Innovations recalls
Official ID 26E068000 · Official record ↗
CPSC · Adult Bed Rails · October 1, 2026
Agrish Reannounces and Expands Recall of Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Additional Units Added
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail …
Company / brand: Zhongshan Lebo Medical Co recalls
Official ID 27014 · Official notice ↗
CPSC · Shower Items · October 1, 2026
Golden Resale Recalls Portable Camping Showers Due to Risk of Serious Injury or Death from Fire Hazard
The recalled camping showers' immersion heaters can quickly ignite when they are partially or completely out of water, posing a risk of serious injury or death from a fire hazard.
Company / brand: Golden Resale recalls
Official ID 27013 · Official notice ↗
CPSC · Powered Pumps · October 1, 2026
Dollar Tree Stores Recalls Electric Balloon Pumps Due to Burn Hazard
The recalled electric balloon pumps can overheat, posing a burn hazard.
Company / brand: Dollar Tree Stores recalls
Official ID 27012 · Official notice ↗
CPSC · Electric Blankets/Warmers · October 1, 2026
Kobayashi Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn hazards.
Company / brand: Kobayashi Consumer Products recalls
Official ID 27011 · Official notice ↗
CPSC · Cleaning Equipment, Inc. Brooms, Mops, Brushes, Etc · October 1, 2026
Walmart Recalls Over 4.4 Million Expert Grill Brushes Due to Ingestion Hazard
Small metal wire bristles can detach from the brushes and stick to the grill or food, posing an ingestion hazard and risk of serious internal injuries that could require surgery.
Company / brand: Walmart recalls
Official ID 27010 · Official notice ↗
CPSC · Electric Blankets/Warmers · October 1, 2026
Gobi Heat Recalls Rechargeable Hand Warmers Due to Risk of Serious Injury from Fire and Burn Hazards
The lithium-ion battery and electrical components in the recalled hand warmers can overheat and ignite, posing a risk of serious injury from fire and burn hazards.
Company / brand: Dragon Gear recalls
Official ID 27009 · Official notice ↗
CPSC · Toy Figures · October 1, 2026
GBYMIUY Recalls Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
The magnetic stick figure toy sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children. When high-po…
Company / brand: Ningbo Jiboyou Trading Co recalls
Official ID 27008 · Official notice ↗
CPSC · Floor Lamps Or Table Lamps, Electric (Excl Halogen) · October 1, 2026
Designs Direct Recalls Cupcakes and Cashmere Brand Three-Light Floor Lamps, Due to Risk of Serious Injury from Fire and Burn Hazards
When plugged in or switched on, the lamp cord or internal wiring can smoke, melt, spark, overheat or ignite, posing a risk of serious injury from fire and burn hazards.
Company / brand: Designs Direct recalls
Official ID 27007 · Official notice ↗
CPSC · Squeeze Or Squeaker Toys · October 1, 2026
LLK Trading Recalls Mochi Malrang Mystery Dumpling Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
The mystery dumpling toys violate the mandatory safety standard for toys because the water beads inside the dumplings expand larger than permitted, posing a deadly ingestion hazard…
Company / brand: LLK Trading recalls
Official ID 27006 · Official notice ↗
CPSC · Adult Bed Rails · October 1, 2026
YunHeng Recalls LandTale Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
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: Landtale Group recalls
Official ID 27005 · Official notice ↗
CPSC · Electric Power-Assisted Pedal Bikes (Excl Offroad/Minibikes) · October 1, 2026
Gazelle USA Recalls Urban Arrow Cargo Electric Bikes Due to Fall Hazard
The front bolt in the seat post clamping mechanism can break, causing the seat to become loose, posing a fall hazard.
Company / brand: Gazelle USA recalls
Official ID 27004 · Official notice ↗
CPSC · Squeeze Or Squeaker Toys · October 1, 2026
ABC Trading Recalls Squishy Toys Due to Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
The squishy toys violate the mandatory safety standard for toys because the water beads inside the toys expand larger than permitted, posing a deadly ingestion hazard. If a water b…
Company / brand: ABC Trading recalls
Official ID 27003 · Official notice ↗
NHTSA · Vehicle · September 30, 2026
Volkswagen Id.4 recall (26V630000)
A vehicle fire increases the risk of injury.
Company / brand: Volkswagen Group recalls
Official ID 26V630000 · Official record ↗
NHTSA · Vehicle · September 30, 2026
Greenpower Motor Company Electrical System recall (26V629000)
The bus moving while the wheelchair lift is in use increases the risk of injury.
Company / brand: Greenpower Motor Company recalls
Official ID 26V629000 · Official record ↗
NHTSA · Vehicle · September 30, 2026
Grech Motors Electrical System recall (26V628000)
An overheated printed circuit board increases the risk of a fire.
Company / brand: Grech Motors recalls
Official ID 26V628000 · Official record ↗
NHTSA · Vehicle · September 30, 2026
Highland Ridge TT Range Lite Air recall (26V627000)
A detached tank can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Highland Ridge RV recalls
Official ID 26V627000 · Official record ↗
NHTSA · Vehicle · September 30, 2026
Starcraft RV TT Super Lite Maxx recall (26V626000)
A detached tank can become a road hazard for other vehicles, increasing the risk of a crash.
Company / brand: Starcraft RV recalls
Official ID 26V626000 · Official record ↗
FDA Not Yet Classified · Drug · September 30, 2026
0 recall — Otsuka ICU Medical LLC
Product Mix-up: 0.9% SODIUM CHLORIDE Injection, USP may potentially contain the overwrap with labeling indicating it to be 0.9% SODIUM CHLORIDE Injection, USP but the actual produc…
Company / brand: Otsuka ICU Medical recalls
Official ID EVT-99892-f8gl50 · Official record ↗
FDA Not Yet Classified · Food · September 30, 2026
Almond Joy Ice Cream Bar recall — Unilever North America Supply Chain Company, LLC
Inaccurate Nutrition Facts information listed on product
Company / brand: Unilever North America Supply Chain Company recalls
Official ID EVT-99757-1erqwvz · Official record ↗
FDA Class II · Medical device · September 30, 2026
Medline Convenience Kits recall — Medline Industries, LP
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could r…
Company / brand: Medline Industries recalls
Official ID Z-3269-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Medline Convenience Kits recall — Medline Industries, LP
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could r…
Company / brand: Medline Industries recalls
Official ID Z-3268-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Medline Convenience Kits recall — Medline Industries, LP
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could r…
Company / brand: Medline Industries recalls
Official ID Z-3267-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Medline Convenience Kits recall — Medline Industries, LP
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could r…
Company / brand: Medline Industries recalls
Official ID Z-3266-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Medline Convenience Kits recall — Medline Industries, LP
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could r…
Company / brand: Medline Industries recalls
Official ID Z-3265-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
PRO+ 40" MRS SURFACE recall — Baxter Healthcare Corporation
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product spec…
Company / brand: Baxter Healthcare recalls
Official ID Z-3264-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
PRO+ 36" MRS SURFACE recall — Baxter Healthcare Corporation
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product spec…
Company / brand: Baxter Healthcare recalls
Official ID Z-3263-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
PRO+ MRS SURFACE FOR VERSACARE recall — Baxter Healthcare Corporation
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved product or product spec…
Company / brand: Baxter Healthcare recalls
Official ID Z-3262-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Halyard IV START KIT NON-STERILE recall — AVID Medical, Inc.
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
Company / brand: AVID Medical recalls
Official ID Z-3261-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Halyard IV START KIT NON-STERILE recall — AVID Medical, Inc.
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
Company / brand: AVID Medical recalls
Official ID Z-3260-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
New York Embroidery Studio Trinity Non-Surgical Isolation Gown recall — New York Embroidery Studio, Inc.
Gowns do not consistently meet the minimum liquid-barrier performance required.
Company / brand: New York Embroidery Studio recalls
Official ID Z-3259-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Cardioroot Woven Collagen Coated Vascular Graft recall — INTERVASCULAR, SAS
Product failed to meet the specified acceptance criteria for Integral Water Permeability (IWP).
Company / brand: INTERVASCULAR recalls
Official ID Z-3258-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Brand Name recall — Baxter Healthcare Corporation
Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to firm and testing confirmed devic…
Company / brand: Baxter Healthcare recalls
Official ID Z-3257-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
REF recall — DeRoyal Industries Inc
Myocardial temperature probes contain an incorrect needle. Specifically, an 18mm needle was included instead of a 15mm needle.
Company / brand: DeRoyal Industries recalls
Official ID Z-3256-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Presource Convenience Kits recall — Cardinal Health 200, LLC
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3255-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Presource Convenience Kits recall — Cardinal Health 200, LLC
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated applicator could result in no patient…
Company / brand: Cardinal Health 200 recalls
Official ID Z-3254-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US recall — Criticare Technologies, Inc.
Complaint trend where "Checkline Error" alarm presents at device setup, rendering the CO2 monitoring function inoperable. May result in procedure delay.
Company / brand: Criticare Technologies recalls
Official ID Z-3253-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Automated Impella Controller (AIC) with the below product descriptions and corresponding P recall — Abiomed, Inc.
Retrospective report of issues remedied in 2019 with firmware and software patches: 1. Defects in optical bench (OPB) firmware V2.19, which affected the accuracy and stability of t…
Company / brand: Abiomed recalls
Official ID Z-3251-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code recall — Becton, Dickinson and Company
Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.
Company / brand: Becton recalls
Official ID Z-3250-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234 recall — Philips Ultrasound, LLC
Due to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood flow velocity measure…
Company / brand: Philips Ultrasound recalls
Official ID Z-3249-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Brand Name recall — CooperVision, Inc.
A small number of lenses within the affected lot are of the incorrect power.
Company / brand: CooperVision recalls
Official ID Z-3248-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector recall — Olympus Corporation of the Americas
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
Company / brand: Olympus of the Americas recalls
Official ID Z-3247-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector recall — Olympus Corporation of the Americas
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
Company / brand: Olympus of the Americas recalls
Official ID Z-3246-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Olympus BiCOAG Hemostasis Probe 10Fr Fixed Pin Connector recall — Olympus Corporation of the Americas
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
Company / brand: Olympus of the Americas recalls
Official ID Z-3245-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector recall — Olympus Corporation of the Americas
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.
Company / brand: Olympus of the Americas recalls
Official ID Z-3244-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
SmartPath to dStream for 1 recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3243-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
MR 7700 and Upgrade to MR 7700 recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3242-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
MR 5300 Model Number (REF) recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3241-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Name (Model Number) recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3240-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Ingenia Elition S and Ingenia Elition X recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3239-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Ingenia 3 recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3238-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Ingenia Ambition S and Ingenia Ambition X recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3237-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Ingenia 1 recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3236-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Evolution upgrade 1 recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3235-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Achieva XR recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3234-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Achieva 3 recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3233-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Achieva 1 recall — Philips North America Llc
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction requirements exceed the…
Company / brand: Philips North America recalls
Official ID Z-3232-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
VITEK 2 AST-N461 TEST KIT recall — Biomerieux Inc
The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe, causing a potential r…
Company / brand: Biomerieux recalls
Official ID Z-3231-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Medline convenience kits containing Healthmark Instrument Channel Brushes recall — Medline Industries, LP
Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards as…
Company / brand: Medline Industries recalls
Official ID Z-3230-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Medline convenience kits containing Healthmark Instrument Channel Brushes recall — Medline Industries, LP
Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards as…
Company / brand: Medline Industries recalls
Official ID Z-3229-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
SeaSpine Mariner Deformity Product Name recall — SEASPINE ORTHOPEDICS CORPORATION
The proximal thread depth of the spinal device is out of design specification.
Company / brand: SEASPINE ORTHOPEDICS recalls
Official ID Z-3226-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors recall — Fresenius Medical Care Renal Therapies Group, LLC
Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed.
Company / brand: Fresenius Medical Care Renal Therapies Group recalls
Official ID Z-3225-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
PowerLED 300 Concealed Lighting System (PWD30+SF W K3 SPRING ARM A2 FC3 50-100nm) Model Nu recall — Maquet SAS
The potential for the device to detach at the junction between the spring arm and suspension arm and fall causing potential injury.
Company / brand: Maquet SAS recalls
Official ID Z-3224-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
REF recall — Ventec Life Systems, Inc.
Labeling; Oxygen Cylinders do not contain required medical gas labeling
Company / brand: Ventec Life Systems recalls
Official ID Z-3223-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
REF recall — Ventec Life Systems, Inc.
Labeling; Oxygen Cylinders do not contain required medical gas labeling
Company / brand: Ventec Life Systems recalls
Official ID Z-3222-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve recall — Ventec Life Systems, Inc.
Labeling; Oxygen Cylinders do not contain required medical gas labeling
Company / brand: Ventec Life Systems recalls
Official ID Z-3221-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Midmark IQvitals Zone recall — Midmark Corporation
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Company / brand: Midmark recalls
Official ID Z-3220-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Midmark IQvitals Zone recall — Midmark Corporation
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Company / brand: Midmark recalls
Official ID Z-3219-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Midmark IQvitals Zone recall — Midmark Corporation
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Company / brand: Midmark recalls
Official ID Z-3218-2026 · 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 ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.