FDA Class II · Drug · July 29, 2026
Glycopyrrolate Oral Solution recall — Precision Dose Inc.
Failed Impurities/Degradation Specifications
Company / brand: Precision Dose recalls
Official ID D-0741-2026 · Official record ↗
Latest recalls — page 16
Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 1,501–1,600, newest first.
FDA Class III · Drug · July 29, 2026
Dabigatran etexilate Capsules recall — Ascend Laboratories, LLC
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testin…
Company / brand: Ascend Laboratories recalls
Official ID D-0736-2026 · Official record ↗
FDA Class III · Drug · July 29, 2026
Dabigatran etexilate Capsules recall — Ascend Laboratories, LLC
Failed Impurities/Degradation Specifications: OOS result was observed during the related substance test analysis with respect to Impurity II, Impurity III and Total impurity testin…
Company / brand: Ascend Laboratories recalls
Official ID D-0735-2026 · Official record ↗
FDA Class I · Drug · July 29, 2026
Cetirizine Hydrochloride Tablets USP 5 mg recall — JB Chemicals and Pharmaceuticals Ltd
Cross Contamination with Other Products: Customer complaints for appearance of discolored tablets and red dots observed on Cetirizine Hydrochloride Tablets USP 5 mg. Determined to …
Company / brand: JB Chemicals and Pharmaceuticals recalls
Official ID D-0732-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Xylocaine (lidocaine HCl Injection recall — Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Company / brand: Fresenius Kabi USA recalls
Official ID D-0729-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Xylocaine (lidocaine HCl Injection recall — Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Company / brand: Fresenius Kabi USA recalls
Official ID D-0728-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Naropin (ropivacaine hydrochloride Injection recall — Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Company / brand: Fresenius Kabi USA recalls
Official ID D-0727-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Lidocaine HCl Injection recall — Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in products
Company / brand: Fresenius Kabi USA recalls
Official ID D-0726-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Glycopyrrolate Injection recall — Fresenius Kabi USA, LLC
Presence of Particulate Matter: Hair was found in product
Company / brand: Fresenius Kabi USA recalls
Official ID D-0725-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rising recall — Rising Pharma Holding, Inc.
Presence of Precipitate: medication was crystallizing and particles floating in the bottle
Company / brand: Rising Pharma Holding recalls
Official ID D-0724-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops Cool Relief (naphazoline hydrochloride 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0722-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops Dry Aid (povidone 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0721-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops Dry Aid (povidone 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0720-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops Digi Eye (hypromellose 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0719-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops Optic Glow (naphazoline hydrochloride 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0718-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0717-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops Max Strength (naphazoline hydrochloride 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0716-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Rohto Cooling Eye Drops ALL-IN-ONE (hypromellose 0 recall — Rohto-Mentholatum (Vietnam) Co., Ltd.
Lack of Assurance of Sterility
Company / brand: Rohto-Mentholatum (Vietnam) Co recalls
Official ID D-0715-2026 · Official record ↗
FDA Class III · Drug · July 29, 2026
Lidolog Kit recall — Asclemed USA Inc.
Labeling: Not Elsewhere Classified: The label wrap covers the barcode, making it hard to scan
Company / brand: Asclemed USA recalls
Official ID D-0713-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Amlodipine and Olmesartan Medoxomil Tablets recall — Ascend Laboratories, LLC
Failed Dissolution Specifications; Olmesartan Medoxomil content below specifications
Company / brand: Ascend Laboratories recalls
Official ID D-0712-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0711-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0710-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0709-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0708-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0707-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0706-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0705-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0704-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0703-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0702-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0701-2026 · Official record ↗
FDA Class II · Drug · July 29, 2026
Levothyroxine Sodium Tablets recall — Major Pharmaceuticals
Subpotent Drug
Company / brand: Major Pharmaceuticals recalls
Official ID D-0700-2026 · Official record ↗
NHTSA · Vehicle · July 28, 2026
Grand Design Imagine recall (26V492000)
An overheated conductor may increase the risk of a fire.
Company / brand: Grand Design RV recalls
Official ID 26V492000 · Official record ↗
NHTSA · Vehicle · July 28, 2026
Grand Design Lineage recall (26V491000)
Incorrect tire pressure information can result in overinflated tires, increasing the risk of tire failure and a crash.
Company / brand: Grand Design RV recalls
Official ID 26V491000 · Official record ↗
NHTSA · Vehicle · July 28, 2026
Grand Design Imagine recall (26V490000)
Contact with wiring may cause a short circuit or an electrical arc, increasing the risk of a fire.
Company / brand: Grand Design RV recalls
Official ID 26V490000 · Official record ↗
NHTSA · Vehicle · July 28, 2026
Ford Motor Company Back Over Prevention recall (26V489000)
An obstructed rearview camera image can reduce the driver's rear visibility, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V489000 · Official record ↗
NHTSA · Vehicle · July 28, 2026
Newell P50 recall (26V488000)
A cracked base may result in a loss of air pressure and suspension support, increasing the risk of a crash.
Company / brand: Newell Coach recalls
Official ID 26V488000 · Official record ↗
NHTSA · Vehicle · July 28, 2026
Ford Mustang Mach E recall (26V487000)
Detached trim pieces can create a road hazard, increasing the risk of a crash.
Company / brand: Ford Motor Company recalls
Official ID 26V487000 · Official record ↗
NHTSA · Vehicle · July 27, 2026
Foretravel Exterior Lighting recall (26V486000)
Brake lights that remain on may fail to alert other vehicles of the driver's intention, increasing the risk of a crash.
Company / brand: Foretravel recalls
Official ID 26V486000 · Official record ↗
NHTSA · Vehicle · July 27, 2026
Paccar Incorporated Electrical System recall (26V485000)
A loss of lighting, windshield wipers, ABS function, or a loss of drive power can increase the risk of a crash.
Company / brand: Paccar Incorporated recalls
Official ID 26V485000 · Official record ↗
NHTSA · Vehicle · July 27, 2026
Jayco Exterior Lighting recall (26V484000)
Brake lights that remain on may fail to alert other vehicles of the driver's intention, increasing the risk of a crash.
Company / brand: Jayco recalls
Official ID 26V484000 · Official record ↗
NHTSA · Vehicle · July 27, 2026
Entegra Anthem recall (26V483000)
Incorrect information may result in the wrong sized replacement tires being installed, increasing the risk of a crash.
Company / brand: Jayco recalls
Official ID 26V483000 · Official record ↗
NHTSA · Vehicle · July 24, 2026
Frontrunner Frontrunner recall (26V482000)
An unsecured wheelchair can move during transit, increasing the risk of injury.
Company / brand: Frontrunner Bus Group recalls
Official ID 26V482000 · Official record ↗
NHTSA · Vehicle · July 24, 2026
Mercedes-Benz Usa Latches/Locks/Linkages recall (26V481000)
A vehicle rollaway increases the risk of a crash or injury.
Company / brand: Mercedes-Benz Usa recalls
Official ID 26V481000 · Official record ↗
NHTSA · Vehicle · July 24, 2026
Yamaha Boat Trailer recall (26V480000)
A detached trailer increases the risk of a crash.
Company / brand: Midwest Industries recalls
Official ID 26V480000 · Official record ↗
NHTSA · Vehicle · July 24, 2026
Arboc Spirit Of Independence recall (26V479000)
The rear spring hanger may detach from the frame, increasing the risk of a crash.
Company / brand: Arboc Specialty Vehicles recalls
Official ID 26V479000 · Official record ↗
NHTSA · Vehicle · July 23, 2026
BMW S 1000 RR recall (26V478000)
An engine stall or failure of electrical systems such as the instrument display or ABS, increases the risk of a crash.
Company / brand: BMW Of North America recalls
Official ID 26V478000 · Official record ↗
NHTSA · Vehicle · July 23, 2026
Forest River Electrical System recall (26V477000)
An overheated printed circuit board increases the risk of a fire.
Company / brand: Forest River recalls
Official ID 26V477000 · Official record ↗
NHTSA · Vehicle · July 23, 2026
Forest River Equipment recall (26V476000)
Incorrect water tank capacity information can allow the vehicle to be overloaded and increase the risk of a crash.
Company / brand: Forest River recalls
Official ID 26V476000 · Official record ↗
NHTSA · Vehicle equipment · July 23, 2026
K&N Replacement Fuel Filter recall (26E048000)
A fuel leak in the presence of an ignition source increases the risk of a fire. In addition, pieces of the O-ring may clog the fuel lines, causing a loss of engine performance and …
Company / brand: K&N Engineering recalls
Official ID 26E048000 · Official record ↗
CPSC · Consumer Product · July 23, 2026
Peony Design Recalls Personalized Baby Bibs and Stroller Bags Due to Risk of Serious Injury or Death from Choking Hazard
The snap can detach from the recalled bibs and stroller bags, posing a risk of serious injury or death from a choking hazard to young children.
Company / brand: Peony Design Co recalls
Official ID 26639 · Official notice ↗
CPSC · Consumer Product · July 23, 2026
CuddleCubs Creations Teething Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by YouRfocus
The recalled teething toy sets contain a pull string teething toy that violates the mandatory standard for toys because the silicone strings are smaller and longer than permitted. …
Company / brand: Foshanshi Kaijinying Dianzishangmao Youxiangongsi (Foshan Kaijinying Electronic Commerce Co recalls
Official ID 26638 · Official notice ↗
CPSC · Consumer Product · July 23, 2026
OeyUoc Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act; Sold Exclusively on Amazon by Yuanxinxiang
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to …
Company / brand: Shenzhen Yuanxinxiang Trade Co recalls
Official ID 26637 · Official notice ↗
CPSC · Consumer Product · July 23, 2026
Sviyatp Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violate Virginia Graeme Baker Pool & Spa Safety Act
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing deadly entrapment and drowning hazards to …
Company / brand: Shenzhen Meilanxiang Trading Co recalls
Official ID 26636 · Official notice ↗
CPSC · Consumer Product · July 23, 2026
Aojieni Silicone Recalls Sili Factory Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys
The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's …
Company / brand: Shenzhen Aojieni Silicone Technology Co recalls
Official ID 26635 · Official notice ↗
CPSC · Consumer Product · July 23, 2026
12-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Romorgniz
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. T…
Company / brand: Xuzhou Mingquanhe Household Co recalls
Official ID 26634 · Official notice ↗
CPSC · Consumer Product · July 23, 2026
EnHomee 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Sold on Walmart.com by Raybee-Direct
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risk of serious injuries or death to children. Th…
Company / brand: Xuzhou Mingquanhe Household Co recalls
Official ID 26633 · Official notice ↗
NHTSA · Vehicle · July 22, 2026
Daimler Trucks North America Exterior Lighting recall (26V475000)
Insufficient low beam headlight illumination can reduce driver visibility, increasing the risk of a crash.
Company / brand: Daimler Trucks North America recalls
Official ID 26V475000 · Official record ↗
NHTSA · Vehicle · July 22, 2026
Heil Side Loader Garbage Truck recall (26V474000)
Electrical component failure may lead to an unexpected vehicle shutdown, increasing the risk of a crash. In addition, an electrical short increases the risk of a fire.
Company / brand: The Heil CO recalls
Official ID 26V474000 · Official record ↗
NHTSA · Vehicle · July 22, 2026
Volkswagen Group Back Over Prevention recall (26V473000)
A rearview camera that fails to display an image can reduce the driver’s view behind the vehicle, increasing the risk of a crash.
Company / brand: Volkswagen Group recalls
Official ID 26V473000 · Official record ↗
NHTSA · Vehicle · July 22, 2026
Coach And Equipment MFG Equipment Adaptive/Mobility recall (26V472000)
A wheelchair lift that continues to move while occupied increases the risk of injury.
Company / brand: Coach And Equipment MFG recalls
Official ID 26V472000 · Official record ↗
NHTSA · Vehicle · July 22, 2026
Aluminum Trailer Company Electrical System recall (26V471000)
A winch that operates unintentionally may increase the risk of injury.
Company / brand: Aluminum Trailer Company recalls
Official ID 26V471000 · Official record ↗
NHTSA · Vehicle equipment · July 22, 2026
Hiab Usa Equipment recall (26E047000)
A cracked weld may result in the collapse of the crane column when in use, increasing the risk of injury to the operator or others nearby.
Company / brand: Hiab Usa recalls
Official ID 26E047000 · Official record ↗
FDA Class II · Medical device · July 22, 2026
ST AIA-Pack Testosterone recall — Tosoh Bioscience Inc
The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could cause falsely elevated…
Company / brand: Tosoh Bioscience recalls
Official ID Z-2746-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Photera 600 3-D recall — Daavlin Distributing Company
Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000).
Company / brand: Daavlin Distributing Company recalls
Official ID Z-2744-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Photera 600 recall — Daavlin Distributing Company
Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000).
Company / brand: Daavlin Distributing Company recalls
Official ID Z-2743-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Photera 400 recall — Daavlin Distributing Company
Calibrated Output was not calculating correctly - UV Sensor GAIN being applied was incorrect - GAIN seemed to be "4/5" instead of "7" (counts were at ~1000 instead of ~5000).
Company / brand: Daavlin Distributing Company recalls
Official ID Z-2742-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System (Model VH-4000 recall — Maquet Cardiovascular, LLC
Getinge identified that Vasoview Hemopro 2 devices from Lot 3000547797 were exposed to an out-of-specification sterilization dose during a gamma sterilization run (Run ID 1183-2878…
Company / brand: Maquet Cardiovascular recalls
Official ID Z-2741-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Brand Name recall — 3B Medical, Inc.
Packaging and labeling discrepancy involving product size identification and associated Unique Device Identifier (UDI/GTIN).
Company / brand: 3B Medical recalls
Official ID Z-2740-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Medtronic Bio-Medicus Adult Cannula Kit recall — Medtronic Perfusion Systems
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2739-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Medtronic DLP One-Piece Pediatric Arterial Cannula recall — Medtronic Perfusion Systems
Medtronic received two complaints of loose foreign material confirmed as containing trace levels of blood.
Company / brand: Medtronic Perfusion Systems recalls
Official ID Z-2738-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ616 recall — Medline Industries, LP
Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of produc…
Company / brand: Medline Industries recalls
Official ID Z-2737-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267 recall — Medline Industries, LP
Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health consequences from use of produc…
Company / brand: Medline Industries recalls
Official ID Z-2736-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Papablic Replacement Brush Heads recall — Papablic Inc
Potential for brush heads to break.
Company / brand: Papablic recalls
Official ID Z-2734-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Papablic Replacement Brush Heads recall — Papablic Inc
Potential for brush heads to break.
Company / brand: Papablic recalls
Official ID Z-2733-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Orthofix MINIRAIL recall — Orthofix U.S. LLC
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
Company / brand: Orthofix U.S recalls
Official ID Z-2732-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF recall — Orthofix U.S. LLC
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
Company / brand: Orthofix U.S recalls
Official ID Z-2731-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Orthofix MINIRAIL recall — Orthofix U.S. LLC
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
Company / brand: Orthofix U.S recalls
Official ID Z-2730-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Orthofix MINIRAIL recall — Orthofix U.S. LLC
Unilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail M122 was labeled as M111
Company / brand: Orthofix U.S recalls
Official ID Z-2729-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Optima XR240amx recall — GE Medical Systems, LLC
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been…
Company / brand: GE Medical Systems recalls
Official ID Z-2728-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Optima XR220amx recall — GE Medical Systems, LLC
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been…
Company / brand: GE Medical Systems recalls
Official ID Z-2727-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Optima XR200amx recall — GE Medical Systems, LLC
GE HealthCare has become aware that in certain Optima XR200/220/240amx systems that have had a column replacement completed, functional testing of the safety pawl may not have been…
Company / brand: GE Medical Systems recalls
Official ID Z-2726-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Rapid Refill Continuous Injection System recall — Boston Scientific Corporation
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold, resulting in loo…
Company / brand: Boston Scientific recalls
Official ID Z-2725-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
ICU Medical Plum Solo Precision IV Pump recall — ICU Medical, Inc.
In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate.
Company / brand: ICU Medical recalls
Official ID Z-2724-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
ICU Medical Plum Duo Infusion Pump recall — ICU Medical, Inc.
In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate.
Company / brand: ICU Medical recalls
Official ID Z-2723-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
da Vinci SP Instrument Arm Drape recall — Intuitive Surgical, Inc.
Robotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the product, which may expose a secti…
Company / brand: Intuitive Surgical recalls
Official ID Z-2722-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Olympus Glass Body for 194 Ellik Evacuator recall — Olympus Corporation of the Americas
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.
Company / brand: Olympus of the Americas recalls
Official ID Z-2721-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Olympus Ellik Evacuator Includes Glass Body recall — Olympus Corporation of the Americas
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.
Company / brand: Olympus of the Americas recalls
Official ID Z-2720-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Olympus Toomey Evacuator 50cc with Adaptor recall — Olympus Corporation of the Americas
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.
Company / brand: Olympus of the Americas recalls
Official ID Z-2719-2026 · Official record ↗
FDA Class II · Medical device · July 22, 2026
Olympus Toomey Evacuator 30cc with Adaptor recall — Olympus Corporation of the Americas
Some sterilization parameters included in the IFU may not consistently render the devices adequately sterile and therefore should no longer be used to sterilize the devices.
Company / brand: Olympus of the Americas recalls
Official ID Z-2718-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
Bone Marrow Tray recall — Argon Medical Devices, Inc
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Company / brand: Argon Medical Devices recalls
Official ID Z-2709-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
Arterial Line Kit 20ga x 6 recall — Argon Medical Devices, Inc
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Company / brand: Argon Medical Devices recalls
Official ID Z-2708-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
T-Lok Bone Marrow Tray recall — Argon Medical Devices, Inc
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Company / brand: Argon Medical Devices recalls
Official ID Z-2707-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
General Biospy Tray recall — Argon Medical Devices, Inc
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Company / brand: Argon Medical Devices recalls
Official ID Z-2706-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
One-Piece Introducer Tray recall — Argon Medical Devices, Inc
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Company / brand: Argon Medical Devices recalls
Official ID Z-2705-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F recall — Argon Medical Devices, Inc
Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility.
Company / brand: Argon Medical Devices recalls
Official ID Z-2704-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
ABIOMED Intro Kit recall — Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2693-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
ABIOMED Insertion Kit recall — Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2692-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
ABIOMED Impella CP Set recall — Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2691-2026 · Official record ↗
FDA Class I · Medical device · July 22, 2026
ABIOMED Impella CP Smart Assist Set recall — Abiomed, Inc.
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visua…
Company / brand: Abiomed recalls
Official ID Z-2690-2026 · 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.