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. 2,520 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,520 in last 12 months

Showing 2196121980 of 52,000 recalls

FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: HEB Taco Seasoning Mix 25% Less Sodium Net Wt. 1.25 OZ Recalled by CH...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Williams Ingredients Recalled by CH Guenther & Sons, Inc Due to Potential...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Winco Foods Recalled by CH Guenther & Sons, Inc Due to Potential Salmonella...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 24, 2019· CH Guenther & Sons, Inc

Recalled Item: Great Value Mild Taco Seasoning Recalled by CH Guenther & Sons, Inc Due to...

The Issue: Products contains an ingredient (cumin) potentially contaminated with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2019· New Standard Device Inc

Recalled Item: 'n'-Hole Post which is a component of the Revolution External Recalled by...

The Issue: The threads on posts stripping out when tensioned during application process.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Revelation with software version VC10 and Biopsy Option Intended...

The Issue: An error can occur when performing a biopsy using the InSpect function. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Online TDM Vancomycin Gen.3 ( 200 tests) Catalog # 06779344190 Recalled by...

The Issue: Inaccurately Low Sample Results

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2019· OMNIlife science Inc.

Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...

The Issue: Acetabular liners failed the oxidation testing performed prior to release....

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

Class II — Potential Health HazardOngoing
DrugJuly 23, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Mometasone Furoate Cream USP Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: GMP Deviations: Glenmark received complaints stating that mometasone fuorate...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate Recalled by...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· DeRoyal Industries Inc

Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...

The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Zeus Scientific, Inc.

Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...

The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...

The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2019· GETINGE US SALES LLC

Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...

The Issue: Reversed expiration and manufacturing date on the label

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...

The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 19, 2019· Philips North America, LLC

Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...

The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...

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

Class II — Potential Health HazardOngoing