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 20921–20940 of 27,462 recalls
Recalled Item: CC cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...
The Issue: May report values outside the published performance specifications for pH....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BG cartridges for IRMA TRUPOINT Blood Gas Analyzer Recalled by LifeHealth,...
The Issue: May report values outside the published performance specifications for pH....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Medical Device Identification Card for SureScan pacemaker...
The Issue: Some Medical Device Identification Cards provided to SureScan pacemaker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Flex Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P/N: 9735023 Recalled by Medtronic Navigation, Inc. Due to Specific use...
The Issue: Specific use conditions can increase the possibility of a screwdriver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turon Shoulder Impaction Fixture The Turon and RSP Recalled by Encore...
The Issue: During the Turon assembly, the impaction forces caused the polymer, black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder Prosthesis Stem Impaction Fixture The Turon Recalled by...
The Issue: During the assembly, the impaction forces caused the polymer, black acetal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONSULT(TM) diagnostics hCG CONTROLS Kit Recalled by Biochemical Diagnostics...
The Issue: CONSULT diagnostics hCG Controls have discrepant storage temperatures listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P/N: 9734856 Recalled by Medtronic Navigation, Inc. Due to Specific use...
The Issue: Specific use conditions can increase the possibility of a screwdriver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MILEX PESSARY KIT Recalled by CooperSurgical, Inc. Due to The products have...
The Issue: The products have been identified to have incorrect size prints on the MILEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT-A-CATH Plastic Hub Needles Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: The label on the lid stock of the individual needle packages for a portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16-Slice (Air) Computed Tomography X-ray systems. Intended to...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beef Extract Powder Recalled by Acumedia Manufacturers, Inc. Due to...
The Issue: Incorrect expiration date on label. Correct expiration date was March 25,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAJ-1606 Instrument Channel Adaptor Recalled by Olympus Corporation of the...
The Issue: small puncture marks in a sterile package for an accessory to an Olympus device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NicoletOne Software v5.94 Recalled by Natus Neurology Inc Due to When using...
The Issue: When using the NicoletOne v5.94 software, after exiting the impedance check...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.