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 29212940 of 52,000 recalls

Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Box Base Recalled by Tornier S.A.S. Due to...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Instrument Check Block Recalled by Tornier...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker HoloBlueprint Application Recalled by Tornier S.A.S. Due to Stryker...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Glenoid Box Lid Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Cross Contamination

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Cross Contamination

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Tolterodine Tartrate Extended-Release Capsules Recalled by The Harvard Drug...

The Issue: Failed Dissolution Specifications: Out of specification results obtained...

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2025· Chattem Inc

Recalled Item: Unisom Recalled by Chattem Inc Due to CGMP Deviations: Nitrosamine Drug...

The Issue: CGMP Deviations: Nitrosamine Drug Substance Related Issue impurity above the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen smart insulin pen Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pens may have been incorrectly assembled therefore users could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...

The Issue: the impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW RSV 24T Product Name: ID NOW Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Medtronic Neuromodulation

Recalled Item: Stimulation RC Clinician Programmer Application Recalled by Medtronic...

The Issue: There is a software issue that can permanently disable communication with an...

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

Class II — Potential Health HazardOngoing