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.

52,000 total recalls
2,645 in last 12 months

Showing 1078110800 of 52,000 recalls

Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Dual Species Self-Contained Biological Indicators Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Medtronic Perfusion Systems

Recalled Item: Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance...

The Issue: An upward trend of complaints in which the Temperature Monitoring Adapter...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Steris Corporation

Recalled Item: VERIFY Steam Test Pack (20 Tests and 20 controls) Item Recalled by Steris...

The Issue: Biological indicator (BI) used to promote growth of the G....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2022· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc Host 2 as follows: Product SMN epoc Host 10736387 Recalled by Siemens...

The Issue: pO2 High Recovery in Quality Control When Adjusted for Barometric Pressure

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2022· Atlantic Management Resources Ltd.

Recalled Item: Neuroquell Plus Recalled by Atlantic Management Resources Ltd. Due to cGMP...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2022· Atlantic Management Resources Ltd.

Recalled Item: Menastil Recalled by Atlantic Management Resources Ltd. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2022· Atlantic Management Resources Ltd.

Recalled Item: Neuroquell Recalled by Atlantic Management Resources Ltd. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2022· Atlantic Management Resources Ltd.

Recalled Item: ProSirona Recalled by Atlantic Management Resources Ltd. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Rifampin Capsules USP Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Failure observed in related...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 12, 2022· Something South African LLC

Recalled Item: Pepper Collection 8 Tube Gift Set - a colorful assortment Recalled by...

The Issue: Due to presence of mold (Aspergillus brasiliensis) and Ochratoxin A.

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 11, 2022· ByHeart, INC.

Recalled Item: By Heart Whole Nutrition Infant Formula Recalled by ByHeart, INC. Due to...

The Issue: Infant formula potentially contaminated with Cronobacter sakazakii

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 9, 2022· NCH Life Sciences LLC

Recalled Item: Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Recalled by NCH Life...

The Issue: CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2022· Smiths Medical ASD Inc.

Recalled Item: CADD Administration Set Recalled by Smiths Medical ASD Inc. Due to There are...

The Issue: There are two potential issues with CADD Infusion System Infusion Sets: (1)...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 8, 2022· TELEFLEX LLC

Recalled Item: Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal...

The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2022· Detect Headquarters

Recalled Item: Detect Covid-19 Test Product/Model Number: 21205 Recalled by Detect...

The Issue: There is an increased chance that the tests from affected lots may give...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2022· TELEFLEX LLC

Recalled Item: Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal...

The Issue: Potential for pilot balloon non-inflation or cuff non-deflation.

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

Class II — Potential Health HazardOngoing