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. 2,504 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,504 in last 12 months

Showing 2474124760 of 52,000 recalls

DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 15mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 17, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS)...

The Issue: An intermittent failure which causes a blender initialization fault upon...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-RFP-456 Recalled by NxStage Medical, Inc....

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-403 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-400 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-402 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· Richard Wolf GmbH

Recalled Item: Richard Wolf Bronchoscope Tubes Recalled by Richard Wolf GmbH Due to There...

The Issue: There is a potential deficiency of the TEXAS Bronchoscope Tube product. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-RFP-454 Recalled by NxStage Medical, Inc....

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-404 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-401 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2018· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow B Solution-RFP-406 Recalled by NxStage Medical, Inc. Due to...

The Issue: PureFlow B Solution smaller chamber of the two chamber bag can burst...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· ASO, LLC

Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...

The Issue: Potential that gauze pads may not be fully sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Conformis, Inc.

Recalled Item: iTotal Hip Replacement System Recalled by Conformis, Inc. Due to The stage 1...

The Issue: The stage 1 and 2 reamer instruments used to prepare fixation for the cup in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing