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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 25921–25940 of 27,462 recalls
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns flexible arterial cannula Recalled by Terumo Cardiovascular Systems...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns high-flow aortic arch cannula Recalled by Terumo Cardiovascular...
The Issue: Flexible Arterial Cannula and High-Flow Aortic Arch Cannula connectors were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are...
The Issue: DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Animas(R) 2020 Insulin Infusion Pump Product Usage: This product is Recalled...
The Issue: Animas has identified a component issue affecting a small supply of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for...
The Issue: Lumenis Ltd is recalling certain models of VersaCut Morcellator devices to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Hybrids Recalled by Diagnostic Hybrids Inc Due to RhMK product...
The Issue: RhMK product fungal contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Creatinine Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is including additional information and instructions in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS ANALYZER II (Software Version 2.5.1 & Below. Product Usage:...
The Issue: Veridex, LLC has received a report that a patient's demographics were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELLTRACKS AUTOPREP System (Software Version 2.4.1 & Below. Product Usage:...
The Issue: Veridex, LLC has received a report that a patient's demographics were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROSURGICAL ENT NEEDLE ELECTRODE Recalled by ConMed Corporation Due to...
The Issue: ConMed received complaints of some devices which had broken through the seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.