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. 2,637 recalls have been distributed to Tennessee in the last 12 months.
Showing 15141–15160 of 29,188 recalls
Recalled Item: Brilliance 40 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Slice (Power) Recalled by Philips Medical Systems (Cleveland)...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 10 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...
The Issue: There is a potential for separation of fiberglass resin which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture....
The Issue: Incorrect measurement results caused by microbial contamination of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemoTrol Level 2- In Vitro Diagnostic Hematology quality control mixture...
The Issue: Incorrect measurement results caused by microbial contamination of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: The PLEX Elite 9000 Recalled by Carl Zeiss Meditec, Inc. Due to Under...
The Issue: Under certain fault conditions, the existing design may expose the operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...
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.
Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...
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.