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. 2,404 recalls have been distributed to Wyoming in the last 12 months.
Showing 22961–22980 of 27,462 recalls
Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....
The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...
The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...
The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...
The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...
The Issue: Reports of unexpected movement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Port Access Kit with MicroClave Clear Connector Recalled by ICU Medical,...
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CURBELL MEDICAL CareSense Wireless Advanced LCD Bed and Chair Monitor...
The Issue: The firm became aware of a potential problem that was initiated by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAP Change Kit w/MicroClave Clear Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cap Change Kit with MicroClave Clear Connector Recalled by ICU Medical, Inc....
The Issue: ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Split Cath III Trays Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST¿CKERT HeaterCooler System 3T Recalled by Sorin Group USA, Inc. Due to On...
The Issue: On August 1, 2014 Sorin Group USA, Inc. informed consignees via letter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas IT 1000 Product Usage: Intended Use: An electronic Recalled by...
The Issue: Potential that test results would be assigned to the wrong Patient ID if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...
The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.