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. 2,492 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,492 in last 12 months

Showing 2840128420 of 52,000 recalls

DrugNovember 28, 2017· Teva Pharmaceuticals USA

Recalled Item: Penicillin V Potassium for Oral Solution Recalled by Teva Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: high out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugNovember 28, 2017· EAI-JR286 INC

Recalled Item: Vertra Elemental Resistance (Octyl Methoxycinnamate 6% Recalled by EAI-JR286...

The Issue: CGMP Deviations: products manufactured in a manner that may impact product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 28, 2017· Alere San Diego Inc. DBA Immunalysis Corporation

Recalled Item: lmmunalysis EDDP Urine Control Set 1 The EDDP Urine Controls Recalled by...

The Issue: The High (125 ng/ml) Control does not meet specification - it has been...

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

Class III — Low RiskOngoing
Medical DeviceNovember 27, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ 2000 Theophylline Product Usage: The Syva¿ Emit¿ 2000 Recalled...

The Issue: Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Ethicon, Inc.

Recalled Item: DERMABOND" PRINEO" Skin Closure System Product Usage: DERMABOND PRINEO...

The Issue: Ethicon discovered that specific lots of DERMABOND"PRINEO"System may not dry...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2017· Cincinnati Sub-Zero Products LLC

Recalled Item: Hemotherm¿ Dual Reservoir Cooler/Heater System Models 400CE and 400MR...

The Issue: Due to FDA's safety communication relating to nontuberculous mycobacteria...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2017· Apollo Endosurgery Inc

Recalled Item: Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: Recalled by...

The Issue: Component of the Lap-Band system was missing from the package

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

Class II — Potential Health HazardOngoing
DrugNovember 21, 2017· Lupin Pharmaceuticals Inc.

Recalled Item: Duloxetine Delayed-Release Capsules USP Recalled by Lupin Pharmaceuticals...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 21, 2017· SANTA JOY ORNAMENT & GIFTWARE CO

Recalled Item: Santajoy Ornament & Giftware Co. Recalled by SANTA JOY ORNAMENT & GIFTWARE...

The Issue: It was discovered that the product units it imported may, at peak levels,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· Covidien LLC

Recalled Item: Rechargeable Li-ion battery used with Puritan Bennett TM 980 Series Recalled...

The Issue: Rechargeable lithium-ion batteries with incorrect firmware that are used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: 10 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2017· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: 15 ML REAGENT CUP Recalled by Horiba Instruments, Inc dba Horiba Medical Due...

The Issue: The ABX PENTRA Reagent Containers do not always sit properly into the...

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

Class II — Potential Health HazardOngoing
DrugNovember 20, 2017· Teva Pharmaceuticals USA

Recalled Item: Amethyst (Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Teva...

The Issue: Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2017· Zydus Pharmaceuticals USA Inc

Recalled Item: Paroxetine Tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 20, 2017· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 3.5 Recalled by RAYSEARCH LABORATORIES AB Due to When calculating...

The Issue: When calculating electron Monte Carlo dose with a very large number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Invivo Corporation

Recalled Item: Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio...

The Issue: While in Full Disclosure playback, a user may inadvertently close the Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Phadia Ab

Recalled Item: Phadia Prime software Recalled by Phadia Ab Due to We want to inform all...

The Issue: We want to inform all Phadia 250 system operators performing EliA Assays not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Integrity R1.2 Recalled by Elekta Limited Due to Potential for positional...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2017· Elekta Limited

Recalled Item: Agility with Integrity R3.2 Recalled by Elekta Limited Due to Potential for...

The Issue: Potential for positional errors following automatic table movement (ATM).

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

Class II — Potential Health HazardOngoing
FoodNovember 17, 2017· Elevation Brands, LLC

Recalled Item: Ian's Gluten Free Original Panko Breadcrumbs Recalled by Elevation Brands,...

The Issue: Product may have been exposed to beetles from a raw material supplier. There...

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

Class III — Low RiskOngoing
Refund