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. 2,480 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,480 in last 12 months

Showing 3278132800 of 52,000 recalls

Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....

The Issue: The firm received complaints claiming the dental material failed to set up....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...

The Issue: A review of packaging revealed the seal integrity of the pouch may be...

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

Class II — Potential Health HazardOngoing
FoodNovember 9, 2016· Seth Ellis Chocolatier, LLC

Recalled Item: Free2b Sun Cups Chocolate. Made With SunButter Sunflower Spread. Packaged...

The Issue: Free2b Foods recalled the Sun Cups Chocolate due to potential contamination...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 9, 2016· Sandoz Inc

Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2016· Sandoz Inc

Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2016· VistaPharm, Inc.

Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2016· Care-Tech Laboratories, Inc.

Recalled Item: Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or...

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

Class III — Low RiskOngoing
Refund
FoodNovember 8, 2016· Chaos and Pain

Recalled Item: CANNIBAL FEROX AMPED Recalled by Chaos and Pain Due to Product was analyzed...

The Issue: Product was analyzed and found to contain 1,3- dimethylbutylamine which was...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· DePuy Orthopaedics, Inc.

Recalled Item: LCS Complete Knee Revision System VVC Insert Product Usage: LCS Recalled by...

The Issue: DePuy Orthopaedics, Inc. is voluntarily recalling one lot of the LCS...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Teleflex Medical

Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...

The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Stryker Medical Division of Stryker Corporation

Recalled Item: Performance-LOAD Ambulance Cot Fastener Stretcher Recalled by Stryker...

The Issue: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2016· Meridian Bioscience Inc

Recalled Item: PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due...

The Issue: Internal testing has demonstrated that the indicated kit lots produce false...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Novation Cemented Plus Femoral Stem Recalled by Exactech, Inc. Due to...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Bayer Healthcare

Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...

The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· Exactech, Inc.

Recalled Item: Alteon Neck Preserving Stem Recalled by Exactech, Inc. Due to Products were...

The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...

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

Class II — Potential Health HazardOngoing