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. 2,314 recalls have been distributed to Wyoming in the last 12 months.
Showing 40921–40940 of 48,219 recalls
Recalled Item: DISP 9730951 STRL SPHERE Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PACK 9731975 TUMOR RESECTION AXIEM CR Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAG 9732315 MOUSE STERILE 15 PK Recalled by Medtronic Navigation, Inc. Due...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIN Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATIENT TRACKER 9733534XOM ENT 1PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAK 9733497 NAV NIM-SPINE PEDICLE ACC KT Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPSY NEEDLE KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INST 9731132 KIT CR DRIVER 5PK Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUMOR RESECTION KIT 9733608 SKULL MOUNT Recalled by Medtronic Navigation,...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PIN Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISP 9730950 STRL SPHERE Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Amia Automated PD systems are used in the treatment Recalled by...
The Issue: System error 01779 is produced when the battery cannot be charged due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTRUMENT TRACKER 9733533XOM ENT 1PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHUNT KIT 9733605 NON-INVASIVE Recalled by Medtronic Navigation, Inc. Due to...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mar Cor Purification Recalled by Mar Cor Purification Due to Mar Cor...
The Issue: Mar Cor Purification manufactured Central Water Plant (CWP) reverse osmosis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Ventralight" ST Mesh with Echo PS" 4"x6" Reorder Number: Recalled by...
The Issue: Pouch holding sterile inflation assembly and inflation adapter may be open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIT 9733516 2.9mm DRILL STERILE Recalled by Medtronic Navigation, Inc. Due...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRAPE 9732722 TUBE STERILE O-ARM 20PK Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUMOR RES. PACK 9733553 AxiEM S.M. Recalled by Medtronic Navigation, Inc....
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Medtronic Navigation, Inc. Due to Medtronic Navigation is...
The Issue: Medtronic Navigation is recalling certain Medtronic single-use, disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.