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. 2,694 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,694 in last 12 months

Showing 40014020 of 52,000 recalls

Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD Synapsys Informatics Solution (Laboratory Solution) Version or Model:...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX Recalled by Becton Dickinson & Co. Due to BD confirmed that...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Hermes Medical Solutions AB

Recalled Item: Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Recalled...

The Issue: Due a potential software/configuration issue that may result is incorrect...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to BD confirmed that...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Cartiva, Inc

Recalled Item: Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm) Recalled...

The Issue: Patients implanted with synthetic cartilage implant, may experience a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Single User Software Version or Model: 441007 Catalog Recalled...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Data Management System Recalled by Becton Dickinson & Co. Due...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number:...

The Issue: High-level disinfection ("HLD") with Acecide-C disinfectant in the Olympus...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475 Recalled...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD EpiCenter Data Management System Version or Model: 440887 Catalog...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 Recalled...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2024· Becton Dickinson & Co.

Recalled Item: BD Phoenix M50 Automated Microbiology System Version or Model: 443624...

The Issue: BD confirmed that product service credentials used by some BD technical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 30, 2024· Deseret Biologicals Inc

Recalled Item: DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules Recalled...

The Issue: Product contains undeclared soy lecithin.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2024· Baxter Healthcare Corporation

Recalled Item: Regadenoson Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Labeling: Missing Label

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2024· INCIPIO DEVICES

Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...

The Issue: Recalled lot does not meet specification and has reported incidents of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 29, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: IBU (ibuprofen) 600 mg tablets Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Tablet/Capsule Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 29, 2024· VIONA PHARMACEUTICALS INC

Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization

The Issue: Crystallization

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund