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. 2,645 recalls have been distributed to Tennessee in the last 12 months.
Showing 10881–10900 of 52,000 recalls
Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...
The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...
The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...
The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TUMS Antacid Recalled by GlaxoSmithKline Consumer Healthcare Holdings LLC...
The Issue: Presence of Foreign Substance: The foreign material is primarily comprised...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxcarbazepine Tablets 600mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Presence of foreign substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular...
The Issue: Packaging sterile barrier has been compromised. Open seals can lead to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Source Administration Set (SAS) used with the Medrad Intego PET Infusion...
The Issue: Black specks may be present on the packaged needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ActiveAid 922 Recalled by Altimate Medical, Inc. Due to Device manufactured...
The Issue: Device manufactured with a component with affects the foldability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premium Quality Shirakiku Fish Sausage Jalapeno Net wt. 9.8 oz. Recalled by...
The Issue: Undeclared collagen (bovine dermis) casing
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Premium Quality Shirakiku Fish Sausage Original Net wt. 9.8 oz. Recalled by...
The Issue: Undeclared collagen (bovine dermis) casing
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2¿ - Recalled...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Trak Clavicle Screws Part Number/Part Description: 40-0136 3.0mm x 80mm...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSS Modular Arthrodesis Nail Recalled by Biomet, Inc. Due to Product missing...
The Issue: Product missing the four small locking collar bolts resulting in extension...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcuTwist Acutrak Compression Screws Part Number/Part Description: AI-0010-S...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daptomycin for Injection 350 mg/vial 1 Single-dose vial Recalled by Accord...
The Issue: Labeling mixup: cartons labeled as Daptomycin 350 mg/vial were found to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Products are labeled as: Skippack Medical Lab SARS-CoV-2 Antigen Rapid...
The Issue: Distribution of SARS-CoV-2 Antigen Rapid Test Kits without FDA market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMINOS Lotus Max (VF11) Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Under certain unlikely circumstances during a fluoroscopic examination, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.