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 42201–42220 of 48,376 recalls
Recalled Item: Snowball Cookies sold under the Lambs Farm brand and packaged Recalled by...
The Issue: The labels do not declare milk, soy, and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shortbread Almond Crescent cookies sold under the Lambs Farm brand Recalled...
The Issue: The labels do not declare milk, soy, and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raspberry Swirl Bread loaf sold under the Lambs Farm brand Recalled by The...
The Issue: The labels do not declare soy allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lemon Butter Cookies sold under the Lambs Farm brand and Recalled by The...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Double Chocolate Butter Cookies sold under the Lambs Farm brand Recalled by...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheerful Cookie Combo containing an assortment of Lemon Butter Cookies...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Famous Butter Cookies sold under the Lambs Farm brand and Recalled by The...
The Issue: The labels do not declare milk and wheat allergens.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORCHESTRA/ORCHESTRA PLUS Programmer Recalled by Sorin Group Italia S.r.l....
The Issue: Sorin has voluntarily issued a notification to physicians related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 1 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 22mm Rotatable Retrieval Device (Box of 10 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWISTER PLUS 26mm Rotatable Retrieval Device (Box of 5 configuration)...
The Issue: Sterility of device may be compromised due to lack of pouch seal integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71058-XX: 04.2mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: lM71059-XX: Indus Screw 04.2mm SelfDrilling. Used to...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Indus Invue Screws: IM71016-XX: 04.5mm Recalled by SpineFrontier, Inc. Due...
The Issue: Mismarked and unmarked screws
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro clear(R) 1 day Sphere (o mafilcon A) Recalled by CooperVision Inc. Due...
The Issue: Lots were labeled with incorrect expiration dates on secondary package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.