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 2774127760 of 29,188 recalls

Medical DeviceNovember 19, 2012· BioHorizons Implant Systems Inc

Recalled Item: AutoTac Delivery Handle Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: The cleaning instructions provided may not be sufficient to remove residual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Bunnell, Inc.

Recalled Item: Patient Circuit used with the Life Pulse High Frequency Ventilator. Recalled...

The Issue: Customer complaints received indicate the heater wire insulation can melt,...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 19, 2012· BioHorizons Implant Systems Inc

Recalled Item: Titanium Tack Starter Kit Recalled by BioHorizons Implant Systems Inc Due to...

The Issue: The cleaning instructions provided may not be sufficient to remove residual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Zimmer, Inc.

Recalled Item: Coonrad/Morrey New Ulnar Revision Kit for Use with Non-Interchangeable...

The Issue: Zimmer is initiating a lot specific recall because affected lots could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2012· Roche Diagnostics Operations, Inc.

Recalled Item: Roche COBAS INTEGRA 400 and 400 plus Analyzer Recalled by Roche Diagnostics...

The Issue: A software security issue with Oracles TNS-Listener component has been...

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

Class III — Low RiskOngoing
Medical DeviceNovember 19, 2012· Zimmer, Inc.

Recalled Item: COONMAD/MORREY TOTAL ELBOW ELBOW COMPONENT REPLACEMENT SET BUSHINGS & PINS...

The Issue: Zimmer is initiating a lot specific recall because affected lots could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Abbott Laboratories, Inc

Recalled Item: Clinical Chemistry Phenobarbital Recalled by Abbott Laboratories, Inc Due to...

The Issue: Abbott Diagnostics is recalling Clinical Chemistry Phenobarbital reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek 11 MM Fully Fluted Reamer Recalled by DePuy Mitek, Inc., a...

The Issue: Specific units of the DePuy Mitek Sterile Reamers are not labeled correctly,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Enterprise 9000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Praxair Inc.

Recalled Item: Praxair Vantage Grab n Go - Gas Cylinder pressure regulator Recalled by...

The Issue: Isolated incidents of ignition inside Grab n' Go cylinders that had been...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 16, 2012· Arjo, Inc. dba ArjoHuntleigh

Recalled Item: Enterprise 8000 Bed Recalled by Arjo, Inc. dba ArjoHuntleigh Due to...

The Issue: ArjoHuntleigh has received reports of unintended movement where the backrest...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2012· Ge Healthcare It

Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...

The Issue: There is a potential for data loss associated with empty path names...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· GE Healthcare It

Recalled Item: GE Centricity PACS Workstation Recalled by GE Healthcare It Due to While...

The Issue: While merging exams in a test instance, merges carry forward in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· EEG Info

Recalled Item: EEG NeuroAmp Recalled by EEG Info Due to Mislabeling

The Issue: EEG Info, Inc. is recalling the EEG Neuroamp device because they have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V100-BGM Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V100 Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Viterion TeleHealthcare Llc

Recalled Item: Viterion TeleHealth Monitor Model Number V500 Recalled by Viterion...

The Issue: Viterion telehealth monitors do not transmit "HI" (above the meter's...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2012· Biomet, Inc.

Recalled Item: Biomet Offset Tibial Tray 2.5 mm Adaptor Recalled by Biomet, Inc. Due to...

The Issue: Biomet investigation identified that the square end of the offset tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare BNP (8-type Natriuretic Peptide) 500 Test kit 02816634...

The Issue: Operating range of the ADVIA Centaur systems is 18¿C to 30¿C (64.4¿F to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2012· Zimmer, Inc.

Recalled Item: Persona Recalled by Zimmer, Inc. Due to All lots of the Persona Cemented...

The Issue: All lots of the Persona Cemented Tibial Drill, 5 Degree Cemented Stemmed...

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

Class II — Potential Health HazardOngoing