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. 2,280 recalls have been distributed to West Virginia in the last 12 months.
Showing 42281–42300 of 48,376 recalls
Recalled Item: Physique Enhancing Science ALPHAMINE Recalled by Physique Enhancing Science...
The Issue: Products contain "Aegeline" an unapproved New Dietary Ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Physique Enhancing Science ENHANCED Recalled by Physique Enhancing Science...
The Issue: Products contain "Aegeline" an unapproved New Dietary Ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220 Recalled by...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile X-ray System Recalled by Shimadzu Medical Systems Due to Shimadzu...
The Issue: Shimadzu Corporation is recalling the Shimadzu Mobile X-ray Sytems (MUX-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: During clinical operation, a malfunction may occur causing a system display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional...
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.
Recalled Item: HemosIL High Abnormal Control 3 UNASSAYED Part Number: 0020003320 Recalled...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mega Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 Recalled by...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...
The Issue: Failed Stability Specifications: this product is below specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Renasys EZ PLUS Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renasys EZ Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa 10-Test because it contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gluten Free 60 vcaps Recalled by Mrm Due to Metabolic Response Modifier...
The Issue: Metabolic Response Modifier (MRM) is recalling Gluten Free 60 vcaps because...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RTC 25-C Inline Aerosol Tee Adapter. Intended to be used Recalled by...
The Issue: Some packages of the RTC 25-C may have been shipped to customers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Broncho Flexible Fiberscope Recalled by Karl Storz Endoscopy America Inc Due...
The Issue: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.