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. 2,461 recalls have been distributed to Wyoming in the last 12 months.
Showing 18461–18480 of 27,462 recalls
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due...
The Issue: Internal testing has demonstrated that the indicated kit lots produce false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is Recalled by...
The Issue: BD is conducting a voluntary product recall of the BD Spinal Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z6Ms transesophageal transducers used on ACUSON SC2000 ultrasound systems...
The Issue: Firm received reports about "acquisition errors" and the deterioration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PNEUGEL(R) TENNIS ELBOW STRAP Recalled by DeRoyal Industries Inc Due to...
The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENNIS ELBOW SUPPORT Recalled by DeRoyal Industries Inc Due to DeRoyal...
The Issue: DeRoyal received complaints of mold on Tennis Elbow Straps.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDRAD Intego PET Infusion System - Pump Intended to deliver Recalled by...
The Issue: Bayer has determined that all current Source Administration Sets (SAS) used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...
The Issue: The device defect associated with this recall may result in HbA1c values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...
The Issue: Due to a customer experiencing complaints on bone fraction of assay not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MANOS EX (CAT#TY-12-101) Product Usage: Carpal Tunnel Release: as a Recalled...
The Issue: The firm failed to notify current customers of IFU update/warning. During a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Cable WA00014A Recalled by Olympus Corporation of the Americas Due to...
The Issue: Software malfunction that results in incorrect generation or display of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOCO Futurabond M+ adhesive Recalled by Voco GmbH Due to Labeling mix-up:...
The Issue: Labeling mix-up: Futurabond M+ DCA (Dual Cure Activator) was marked labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adiprep Adipose Transfer System. Product Codes: 51431 Recalled by Terumo...
The Issue: Terumo BCT announces a voluntary field action for the Harvest : Adiprep...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential safety issue where certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens is releasing a software update that provides bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.