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. 2,710 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,710 in last 12 months

Showing 601620 of 29,188 recalls

Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: H pylori (Peptic ulcer) Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Orthofix U.S. LLC

Recalled Item: Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" Recalled by...

The Issue: Labeling contains claims that are not consistently present.

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

Class III — Low RiskOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Neurotransmitters Basic Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: D-Dimer Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Syphilis Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Female Fertility Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Pollen Allergy Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Gonorrhea test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Neurotransmitters Plus Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Adrenal Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Parasite Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Fructose Intolerance Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Cholesterol Test Recalled by GET TESTED INTERNATIONAL AB Due to Distribution...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: GI Microbiome Profile XL Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· Fresenius Kabi USA, LLC

Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Downstream Occlusion alarms may occur during procedures using low flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Iron Deficiency Test (ferritin) Recalled by GET TESTED INTERNATIONAL AB Due...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Diabetes Test (ketones & glucose) Recalled by GET TESTED INTERNATIONAL AB...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2025· GET TESTED INTERNATIONAL AB

Recalled Item: Women s Hormone Test Recalled by GET TESTED INTERNATIONAL AB Due to...

The Issue: Distribution without premarket approval/clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software...

The Issue: A software timing and processor communication issue in MiniMed" 780G...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2025· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX850. Product Number: 866470. Recalled by...

The Issue: Potential issue where the IntelliVue monitors did not alarm.

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

Class II — Potential Health HazardOngoing