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. 989 recalls have been distributed to West Virginia in the last 12 months.
Showing 20381–20400 of 48,376 recalls
Recalled Item: Bubbies Mochi Ice Cream -Strawberry Item Code CS800014 Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream -Green Tea Item Code CS800056 Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Cookie Dough Ice Cream Bites - Brownie Batter Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream -Blood Orange Item Code CS800490 Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream -lychee Item Code CS800001 Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Cookie Dough Ice Cream Bites -Sugar Cookie Item Code CDR00004...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...
The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for Recalled by SCA...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...
The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 73 mm Item # 195756 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 71 mm Item # 195755 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP- CR Tibial Tray- Interlok 59mm Item # 195268 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 59 mm Item # 195750 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9653 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9615 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-CR Tibial Tray - Interlok 87 mm Item # 195278 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 67 mm Item # 195247 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 65 mm Item # 195752 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 71 mm Item # 195249 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 87 mm Item # 195760 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.