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. 1,077 recalls have been distributed to Wyoming in the last 12 months.
Showing 2381–2400 of 27,462 recalls
Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Recalled...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...
The Issue: Complaints have been received regarding post-operative implant collapse.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tacy Medical Recalled by Trinity Sterile, Inc. Due to Potential...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISIONIST CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP with SmartAssist Recalled by Abiomed, Inc. Due to Optical Sensors...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due to...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Select Series Angled Tip Arterial Cannula Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist Recalled by Abiomed, Inc. Due to Optical...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pediatric One-Piece Arterial Cannulae Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nuwellis AquaFlexFlow UF 500 Plus Recalled by Nuwellis Inc Due to The...
The Issue: The AquaFlexFlow UF 500 Plus extracorporeal blood circuit used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.