Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 14501–14520 of 27,462 recalls
Recalled Item: ARTIS zee biplane systems with Material 10094141- a Angiographic x-ray...
The Issue: Vibrations of the C-arm of the plane B may result in reduced image quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly may incorrectly extend the on-analyzer stability time for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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 6 Slice (Air) Recalled by Philips Medical Systems (Cleveland) Inc...
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: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...
The Issue: Falsely elevated (false positive) urobilinogen patient results due to an...
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: 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: 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: 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 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 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: 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-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: 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-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-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: 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: 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: 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.