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. 2,536 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,536 in last 12 months

Showing 2112121140 of 29,188 recalls

Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Applied Medical Technology Inc

Recalled Item: Wilson Penile Implantation System Retractor Frame Recalled by Applied...

The Issue: The firm received a complaint of an open pouch which breaches the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Applied Medical Technology Inc

Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...

The Issue: The firm received a complaint of an open pouch which breaches the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential safety issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: EZ adjust aluminum crutch under the following labels: 1) EZ Recalled by...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Aluminum crutch under the following labels: 1) Aluminum crutch Recalled by...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Acorn Stairlifts Inc

Recalled Item: Acorn 180 Curved Stairlift Recalled by Acorn Stairlifts Inc Due to Aluminum...

The Issue: Aluminum rivets holding the base squab to the framer under prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal Quick Adjust under the following labels: 1) Aluminum crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Applied Medical Technology Inc

Recalled Item: Wilson Implantation System Product Usage: Indicated to aid in tissue...

The Issue: The firm received a complaint of an open pouch which breaches the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Universal aluminum crutch Recalled by Medical Depot Inc. Due to Tip crutch...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Medical Depot Inc.

Recalled Item: Direct Supply aluminum crutch Recalled by Medical Depot Inc. Due to Tip...

The Issue: Tip crutch failure involving the bottom of the metal portion which comes in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2016· Applied Medical Technology Inc

Recalled Item: TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC...

The Issue: The firm received a complaint of an open pouch which breaches the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...

The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 16, 2016· Synthes (USA) Products LLC

Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...

The Issue: Labeling does not match the cleared indications for use in the United States...

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

Class II — Potential Health HazardOngoing