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 22301–22320 of 27,462 recalls
Recalled Item: Malleable C- Retractor Recalled by Synthes, Inc. Due to Potential failure...
The Issue: Potential failure and/or corrosion of the internal spring of the retractor,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicTumorEx 1.0 nordicTumorEx is an image processing software package to...
The Issue: An error was discovered in the interpretation of certain DICOM header tags...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MUM-1 (Multiple myeloma oncogene-1) Recalled by Biocare Medical Llc Due to...
The Issue: Three lots of MUM-1 may not meet their labeled shelf life, as a drop in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Creatinine Reagent Catalog number C7539-150 in vitro...
The Issue: Creatinine kit C7539-150 contains Creatinine reagent R1 that is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal...
The Issue: Teleflex Medical has issued an advisory notification for the RUSCH Curved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TASP) Tibial Articular Surface Provisional Shim Recalled by Zimmer,...
The Issue: Potential for delay in surgery and/or ball bearings to be left in the wound....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autopen Classic Automatic insulin delivery pen Recalled by Owen Mumford USA,...
The Issue: The dials in the Autopens are not working - the dial does not stay dialed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis-8 Peripheral Infusion System. Models CVT808015 Recalled by...
The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01 Recalled...
The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The I-Cart is used to store Recalled by Richard Wolf Medical Instruments...
The Issue: The transformers installed on carts used for Richard Wolf medical video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Integrated APD Set with Cassette 3-Prong Recalled by Baxter...
The Issue: Baxter is issuing a recall for one lot of Integrated Automated Peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Brilliance and Ingenuity Computed Tomography X-ray systems Recalled...
The Issue: Improper assembly of the vertical motor/brake system may lead to uncommanded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional -...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 Vision Side Cart (VSC) used in conjunction with the Recalled by...
The Issue: Intuitive Surgical is initiating a voluntary correction related to da Vinci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Recalled by...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G- Series Beds Recalled by Invacare Corporation Due to Invacare identified...
The Issue: Invacare identified that the rail mounting bracket on the G29 full length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...
The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...
The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.