Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,096 recalls have been distributed to Virginia in the last 12 months.
Showing 13061–13080 of 53,829 recalls
Recalled Item: PEANUT BUTTER CHOCOLATE FUDGE BAR - 8 oz. Recalled by Fudgeamentals LLC Due...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Red Button Vintage Creamery Canadian Vanilla Ice Cream Recalled by Casper's...
The Issue: Burnt Almond Fudge ice cream was packaged into Canadian Vanilla tubs during...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PEANUT BUTTER FUDGE BAR (24-8OZ) FUDGEAMENTALS Recalled by Fudgeamentals LLC...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1. PEANUTTIEST CARAMEL CHOCOLATE P-MADE(6SS)6LB NT WT - not consumer...
The Issue: Fudge contains peanut butter that is potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not consumer...
The Issue: Fudge contains peanut butter that is potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Homeopathic EarAche Ear Drops Recalled by Grato Holdings, Inc. Due to...
The Issue: Microbial contamination of non-sterile product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...
The Issue: Marketed Without An Unapproved NDA/ANDA: Product lot found to be tainted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri Ajo King con Ortiga y Omega 3 Tablets Recalled by Walmart Inc Due to...
The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...
The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Earache Drops Recalled by Grato Holdings, Inc. Due to Microbial...
The Issue: Microbial contamination of non-sterile product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Homeopathic EarAche Drops Recalled by Grato Holdings, Inc. Due to Microbial...
The Issue: Microbial contamination of non-sterile product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethanol for Injection 95% Recalled by US Specialty Formulations LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: B-Complex + Chromic Chloride (Choline Chloride 3% Recalled by US Specialty...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MiniMed 720G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 740G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 620G Insulin Pump (O.U.S. version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G Insulin Pump (U.S. and Canada Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 780G Insulin Pump (O.U.S. Version) Recalled by Medtronic MiniMed Due...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 770G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 670G Insulin Pump (U.S. and O.U.S. Version) Recalled by Medtronic...
The Issue: Due to battery cap deterioration, this may potentially result in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.