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. 2,448 recalls have been distributed to Wyoming in the last 12 months.
Showing 19901–19920 of 27,462 recalls
Recalled Item: Short Percutaneous Antenna with Thermosphere" Technology Standard...
The Issue: Medtronic is voluntarily recalling specific item codes and production lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver Receiver Part Number: MT22430...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G4 PLATINUM Receiver Receiver Part Number: MT20649 Receiver (mg/dL)...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G5 Mobile Receiver Receiver Part Number: MT22719 Receiver (mg/dL)...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G4 PLATINUM (Professional) Receiver Receiver Part Number: MT20649...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator Recalled by...
The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i oxygenators Custom tubing packs for the oxygenator Recalled by...
The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G4 PLATINUM (Pediatric) Receiver with Share Receiver Part Number:...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLS Set Advanced with BIOLINE Coating Custom tubing packs for the oxygenator...
The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Tubing Packs Custom tubing pack for oxygenators Recalled by Maquet...
The Issue: Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G4 PLATINUM Receiver with Share Receiver Part Number: MT22495...
The Issue: Customers may not receive an intended audible alarm or alert if relying on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reveal LINQ insertable Cardiac Monitor Recalled by Medtronic Inc. Due to...
The Issue: Medtronic has identified an issue with the sensitivity of an algorithm used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST RIO Offset Shell Impactor For use by orthopedic Recalled by...
The Issue: Potential disassociation of the orientation pin.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#:...
The Issue: Innovative Ophthalmic Products (IOP) is recalling the Molteno 3 G-Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Duodenoscope Recalled by Pentax Medical Company Due to Pentax Medical...
The Issue: Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Pentra 400 (version 5.0.8 or lower) The ABX PENTRA Recalled by Horiba...
The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 Recalled by Horiba...
The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis (system Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Possible leak in the cooling system, fluids could potentially seep into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sure Vue Color Staph 150T Recalled by Integrated Science Systems Inc Due to...
The Issue: Customer complaints of very weak reactions with the kit, or false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software issues on Cios Alpha mobile C-Arm system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.