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. 1,729 recalls have been distributed to West Virginia in the last 12 months.
Showing 39621–39640 of 48,376 recalls
Recalled Item: Temozolomide active pharmaceutical ingredient packaged in varying grams or...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clomipramine HCI active pharmaceutical ingredient packaged in varying grams...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Procaine HCl active pharmaceutical ingredient packaged in varying grams or...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zoledronic Acid active pharmaceutical ingredient packaged in varying grams...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine HCI active pharmaceutical ingredient packaged in varying grams or...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone active pharmaceutical ingredient packaged in varying grams or...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate active pharmaceutical ingredient packaged in varying grams...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levodopa or L-Dihydroxyphenylalanine active pharmaceutical ingredient...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sevelamer HCl active pharmaceutical ingredient packaged in varying grams or...
The Issue: Penicillin Cross Contamination: All lots of all products repackaged and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ABX PENTRA Reagent Container Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: HORIBA Medical is recalling the ABX PENTRA 400 Reagent Container because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml...
The Issue: Use of the product could result in inadequate recovery of Legionella...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLUTTER Percussor respiratory device Recalled by Aptalis Pharmatech Inc. Due...
The Issue: Customer notification that the device may be difficult to open or close.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView model number: 882478 BrightView X model number: 882480 BrightView...
The Issue: Unintended detector and gantry movement due to software issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I.M. Hole Locator Instrument. Orthopedic manual surgical instrument. The IM...
The Issue: Use of excessive force when impacting may lead to intra-operative femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beachbody Hardcore Base Shake Lot #42932B22 Recalled by Beachbody Llc Due to...
The Issue: During an investigation of label issuance and reconciliation at the firm's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GENTAMICIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Defective...
The Issue: Defective Container: Vials may be missing stoppers.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pediatric Recalled by Cure Medical LLC Due to Some of the intermediate boxes...
The Issue: Some of the intermediate boxes within lot 140417-3, were labeled as P8, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b)...
The Issue: A design deficiency was discovered whereby the Drill/Awl Sleeve and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT/CHILD Radiotransparent Electrode Recalled by Heart Sync, Inc. Due to...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotranslucent Electrode Recalled by Heart Sync, Inc. Due to Heart...
The Issue: Heart Sync Multi-function defibrillation electrodes will not connect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.