Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,638 recalls have been distributed to Tennessee in the last 12 months.
Showing 12481–12500 of 52,000 recalls
Recalled Item: 1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. Recalled by...
The Issue: made with peanut butter contaminated with Salmonella
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: PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS Recalled by Fudgeamentals...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VARIETY TRAY (16 OZ) (C-CNC-PBC) 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: PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS Recalled by...
The Issue: made with peanut butter contaminated with Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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: 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: 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: 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: 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: 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: 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: 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 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 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.
Recalled Item: MiniMed 640G 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 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: CustMbite Recalled by Dental Choice Holding Llc Due to The device was...
The Issue: The device was marketed and sold in the US without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.