Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,492 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,492 in last 12 months

Showing 1338113400 of 48,376 recalls

Medical DeviceDecember 9, 2021· Getinge Usa Sales Inc

Recalled Item: Vaporizer Sevoflurane Maquet Filling Recalled by Getinge Usa Sales Inc Due...

The Issue: A potential chemical degradation of Sevoflurane by Lewis acids (metal oxides...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray...

The Issue: Potential safety issue under specific preconditons that may result in a user...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 8, 2021· Teva Pharmaceuticals USA

Recalled Item: Brinzolamide Ophthalmic Suspension Recalled by Teva Pharmaceuticals USA Due...

The Issue: Defective Container: The notch in the cap that fits into the nozzle of the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 8, 2021· R82 A/S

Recalled Item: R82 by ETAC Push Brace for High-Low Recalled by R82 A/S Due to The chrome...

The Issue: The chrome surface of the push brace can crack during use, potentially...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2021· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: There is a high risk of the blue hub detaching from the corkscrew needle,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 7, 2021· Direct Rx

Recalled Item: Diclofenac Sodium Topical Solution 1.5% Recalled by Direct Rx Due to...

The Issue: Defective Container: Leaking containers.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 7, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...

The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Phenylephrine HCl/Tropicamide Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Dibutyl Squaric Acid Recalled by Edge Pharma, LLC Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Edetate Disodium (EDTA) Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: Edetate Disodium (EDTA) Recalled by Edge Pharma, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2021· Edge Pharma, LLC

Recalled Item: MVASI Recalled by Edge Pharma, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund