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. 2,115 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,115 in last 12 months

Showing 741760 of 29,188 recalls

Medical DeviceOctober 9, 2025· B-K Medical A/S

Recalled Item: bk3500 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...

The Issue: GE HealthCare has become aware that the Instructions for Use within the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Recalled...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Myofunctional Research Company USA

Recalled Item: Myosa for Kids KS1 /Sp/Mb/Mp/Lb/Lc KS2 /Sc/Mb/Mc/Mp/Lb/Lc Myosa Recalled by...

The Issue: Due to firm mistakenly distributing product within the U.S. without FDA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2025· Thoratec LLC

Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone)...

The Issue: Due to potential corrosion issues associated with the Backup Battery cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...

The Issue: The device may either fail to start up, or the transducer may start briefly...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2025· Cellavision AB

Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...

The Issue: Automated cell-locating device barcode reader may read the barcode of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· NeuroLogica Corporation

Recalled Item: GM85 Digital Mobile X-ray imaging System Recalled by NeuroLogica Corporation...

The Issue: The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· Meridian Bioscience Inc

Recalled Item: Meridian Bioscience Recalled by Meridian Bioscience Inc Due to The cap on...

The Issue: The cap on the reaction buffer tube may be missing the black rubber gasket...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· Trividia Health, Inc.

Recalled Item: Good Neighbor Pharmacy Recalled by Trividia Health, Inc. Due to...

The Issue: Manufacturing defect causing LCD display issues with missing or partial...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· Meridian Bioscience Inc

Recalled Item: Meridian Bioscience Recalled by Meridian Bioscience Inc Due to The cap on...

The Issue: The cap on the reaction buffer tube may be missing the black rubber gasket...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2025· Philips Respironics, Inc.

Recalled Item: SimplyGo Mini Recalled by Philips Respironics, Inc. Due to Certain serial...

The Issue: Certain serial numbers of the SimplyGo Mini standard battery kit contain a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC

Recalled Item: OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control...

The Issue: A labeling error was identified on the affected product. The expiration date...

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

Class III — Low RiskOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Oak Mix Specific Allergen Recalled by Siemens Healthcare...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: 3gAllergy Specific IgE Universal Kit Recalled by Siemens Healthcare...

The Issue: The barcode orientation on affected devices causes incorrect scanning order...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Olympus Corporation of the Americas

Recalled Item: Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400...

The Issue: Sterility compromised from small holes that may occur during packaging of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2025· Applied Medical Technology Inc

Recalled Item: Applied Medical Technology Recalled by Applied Medical Technology Inc Due to...

The Issue: The nasal feeding tube may be occluded

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

Class II — Potential Health HazardOngoing