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. 1,658 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
1,658 in last 12 months

Showing 4392143940 of 48,376 recalls

Medical DeviceJune 19, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Suction Wand Recalled by Edwards Lifesciences, LLC Due...

The Issue: Edwards is recalling certain lots of Rigid Suction Wands because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: Free Lock Femoral Hip Fixation System Compression Lag Screw . Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Philips Healthcare Inc.

Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Healthcare...

The Issue: The MRx may deliver a non-synchronized cardioversion shock resulting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Recalled by...

The Issue: Siemens is conducting a field correction for Dimension Vista 500 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery IGS 730 Cardiovascular X-Ray Imaging System. The...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

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

Class II — Potential Health HazardOngoing
DrugJune 19, 2013· Astellas Pharma US Inc

Recalled Item: AmBisome (amphotericin B) liposome for injection Recalled by Astellas Pharma...

The Issue: Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: Theraflu Exte (dextromethorphan hydrobromide 20 mg Recalled by Novartis...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: Theraflu Sugar-Free Nighttime Severe Cold & Cough (acetaminophen 650 mg...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: Theraflu Cold and Flu (acetaminophen 325 mg Recalled by Novartis Consumer...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: Theraflu Daytime Severe Cold & Cough (acetaminophen 650 mg Recalled by...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: Theraflu Multi-Symptom Severe Cold (acetaminophen 500 mg Recalled by...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: Theraflu (acetaminophen 325 mg Recalled by Novartis Consumer Health Due to...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: NeoCitran Extra Strength Cold & Flu (acetaminophen 650 mg Recalled by...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Discoloration: This recall is being carried out due to an orange to brown...

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

Class III — Low RiskOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: NeoCitran (acetaminophen 1000 mg Recalled by Novartis Consumer Health Due to...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: NeoCitran Extra Strength (acetaminophen 650 mg Recalled by Novartis Consumer...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund