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. 2,266 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,266 in last 12 months

Showing 4574145760 of 48,376 recalls

Medical DeviceJanuary 25, 2013· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN...

The Issue: Covidien is correcting labeling to clarify the operational life of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Edwards Lifesciences, LLC

Recalled Item: Proplege Coronary Sinus Catheter model PR9 Recalled by Edwards Lifesciences,...

The Issue: Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Mc-NEIL-PPC, Inc.

Recalled Item: KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is Recalled...

The Issue: This product is not cleared for marketing in the US.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 25, 2013· Mc-NEIL-PPC, Inc.

Recalled Item: KY TINGLING JELLY Personal Lubricant. The product is packaged into Recalled...

The Issue: This product is not cleared for marketing in the US.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2013· Cenorin, LLC

Recalled Item: HLD System Recalled by Cenorin, LLC Due to The temperature sensor/control...

The Issue: The temperature sensor/control system in the HLD Systems Model 610 may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2013· Stelkast Co

Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...

The Issue: Firm was made aware of incidents relating to the difficulty of properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...

The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 24, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...

The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...

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

Class III — Low RiskOngoing
DrugJanuary 23, 2013· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 10% and Sulfur 5% Lotion Recalled by Mission Pharmacal...

The Issue: Superpotent: Drug product active ingredients were formulated incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 23, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Presence of Foreign Tablets/Capsules: Recall is being conducted due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 23, 2013· Procter & Gamble Hair Care Llc

Recalled Item: Crest PRO-HEALTH CPC Antigingivitis/Antiplaque Oral Rinse Recalled by...

The Issue: Cross Contamination with Other Products: Product was mixed with another type...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 23, 2013· Bion Enterprises Ltd

Recalled Item: Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Recalled by...

The Issue: Affected products have a labeled expiration date of one year too long.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 23, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...

The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2013· Bard Peripheral Vascular Inc

Recalled Item: MICROSHEATH¿ - 0.066 (1.7mm) proximal Recalled by Bard Peripheral Vascular...

The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2013· Bard Peripheral Vascular Inc

Recalled Item: USHER¿ Support Catheter- Angled Tip WL130cm Recalled by Bard Peripheral...

The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...

The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2013· Bion Enterprises Ltd

Recalled Item: Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Recalled...

The Issue: Affected products have a labeled expiration date of one year too long.

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

Class III — Low RiskOngoing
Medical DeviceJanuary 23, 2013· Bion Enterprises Ltd

Recalled Item: Plastic bottle containing 10.5 mL of IgM Conjugate Product Usage: Recalled...

The Issue: Affected products have a labeled expiration date of one year too long.

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

Class III — Low RiskOngoing
DrugJanuary 22, 2013· Fresenius Kabi USA LLC (FK USA)

Recalled Item: IRINOTECAN HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA LLC (FK...

The Issue: Crystallization: Active pharmaceutical ingredient is precipitating in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2013· RX South LLC DBA RX3 Pharmacy

Recalled Item: Medi-bolic Booster Injectable (methionine 8.3 mg/mL Recalled by RX South LLC...

The Issue: CGMP Deviations: Pharmaceutical for injection was not manufactured according...

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

Class II — Potential Health HazardOngoing
Refund