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. 2,645 recalls have been distributed to Tennessee in the last 12 months.

52,000 total recalls
2,645 in last 12 months

Showing 1294112960 of 29,188 recalls

Medical DeviceOctober 24, 2019· Centurion Medical Products Corporation

Recalled Item: Centurion Medical Products UNIVERSAL LINE FULL BODY DRAPE KIT - Recalled by...

The Issue: Sterile packaging incomplete seals may compromise sterility of the product

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2019· Sonendo Inc

Recalled Item: GENTLEWAVE Recalled by Sonendo Inc Due to The console would continue to run...

The Issue: The console would continue to run for extended period when the foot pedal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2019· Abbott GmBH & Co. KG

Recalled Item: Alinity c Carbon Dioxide Reagent Kit Recalled by Abbott GmBH & Co. KG Due to...

The Issue: Abbott internal studies have determined that atmospheric Carbon Dioxide...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to The firm...

The Issue: The firm received complaints that the EMPOWR Acetabular Impactor Balls were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer...

The Issue: The locking pin of the front wheel asse mbly of the Evolution Transfer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Eagle 3000 Sterilizer Recalled by Steris Corporation Due to Potential for...

The Issue: Potential for the incorrect pressure safety valve being included in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Edwards Lifesciences, LLC

Recalled Item: EZ Glide Aortic Cannula Recalled by Edwards Lifesciences, LLC Due to Their...

The Issue: Their is a possibility that the cannula may separate from its connector,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: DxM 1096 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: DxM 1040 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Beckman Coulter Inc.

Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...

The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: JAPAN CELL SAVER ELITE SET - 225ML - Product Usage: Recalled by Haemonetics...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: JAPAN DISP SET Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS Elite Fastpack Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: Japan DISP SET Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS Elite Fastpack Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing