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. 2,580 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,580 in last 12 months

Showing 1950119520 of 29,188 recalls

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· 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: 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· 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· 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 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 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· Siemens Medical Solutions USA, Inc.

Recalled Item: Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems...

The Issue: Firm received reports about "acquisition errors" and the deterioration of...

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· 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
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: PNEUGEL(R) TENNIS ELBOW STRAP Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2016· DeRoyal Industries Inc

Recalled Item: TENNIS ELBOW SUPPORT Recalled by DeRoyal Industries Inc Due to DeRoyal...

The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.

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

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

Recalled Item: AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner...

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· Becton Dickinson & Company

Recalled Item: BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is Recalled by...

The Issue: BD is conducting a voluntary product recall of the BD Spinal Anesthesia...

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

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

Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...

The Issue: The device defect associated with this recall may result in HbA1c values...

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

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

Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...

The Issue: Due to a customer experiencing complaints on bone fraction of assay not...

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

Class III — Low RiskOngoing
Medical DeviceNovember 4, 2016· Thayer Intellectual Property, Inc.

Recalled Item: MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a Recalled...

The Issue: The firm failed to notify current customers of IFU update/warning. During a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· Voco GmbH

Recalled Item: VOCO Futurabond M+ adhesive Recalled by Voco GmbH Due to Labeling mix-up:...

The Issue: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· Olympus Corporation of the Americas

Recalled Item: HF Cable WA00014A Recalled by Olympus Corporation of the Americas Due to...

The Issue: Software malfunction that results in incorrect generation or display of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2016· Terumo BCT, Inc.

Recalled Item: Adiprep Adipose Transfer System. Product Codes: 51431 Recalled by Terumo...

The Issue: Terumo BCT announces a voluntary field action for the Harvest : Adiprep...

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

Class II — Potential Health HazardOngoing