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 2846128480 of 29,188 recalls

Medical DeviceJune 16, 2012· DeRoyal Industries Inc

Recalled Item: Custom surgical kits and trays: GEO-MED TOTAL KNEE PACK PGYBK Recalled by...

The Issue: Surgical kits and trays contain Stryker Hytrel Togas which were recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Diagnostica Stago, Inc.

Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...

The Issue: Following a single customer complaint that incorrect INR values were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent...

The Issue: The recall was initiated because Carefusion has identified a potential risk...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Octane-C Cervical Recalled by Exactech, Inc. Due to Exactech, Inc. initiated...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...

The Issue: Hitachi discovered a software error with a feature called Multi-Planar...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Angiodynamics Worldwide Headquarters

Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...

The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Exactech, Inc.

Recalled Item: Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total...

The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2012· Ge Healthcare It

Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...

The Issue: Multiple issues were identified with the GE Centricity PACS-IW system that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2012· Integra Life Sci.

Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...

The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2012· Philips Healthcare Inc.

Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...

The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 13, 2012· Genzyme Corporation

Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...

The Issue: Sterility of product may be compromised due to packaging defect

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Maquet Cardiovascular Us Sales, Llc

Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...

The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2012· Teleflex Medical

Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...

The Issue: Speaker Failure. If the speaker fails and an event occurs which would...

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

Class II — Potential Health HazardOngoing