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. 2,279 recalls have been distributed to Wyoming in the last 12 months.
Showing 45681–45700 of 48,219 recalls
Recalled Item: Reumofan Plus Recalled by Reumofan Plus USA Due to Undeclared Active
The Issue: Marketed without an approved NDA/ANDA: Product may contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg Recalled by...
The Issue: Failed Dissolution Specifications; 8-hours for the 18-month stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: Mitosol (mitomycin for solution) Recalled by Mobius Therapeutics LLC Due to...
The Issue: Non-Sterility: one or more components of the kit have been found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: Growth Factor Complex 200 GFC 200 Recalled by EonNutra, LLC Due to Eon...
The Issue: Eon Nutra, LLC is recalling certain SOTO Supplements GFC 200 because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: Rugby NATURAL IRON SUPPLEMENT Ferrous Sulfate Recalled by Advance...
The Issue: Labeling; Label Mixup; bottles of Ferrous Sulfate actually contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HILLYARD Recalled by Hillyard GMP Due to Microbial Contamination of...
The Issue: Microbial Contamination of Non-Sterile Products: The product may be...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: Lac-Hydrin (ammonium lactate) Lotion Recalled by Ranbaxy Inc. Due to...
The Issue: Crystallization: Recall is due to a non-characteristic gritty/sandy texture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lac-Hydrin (ammonium lactate) Cream Recalled by Ranbaxy Inc. Due to...
The Issue: Crystallization: Recall is due to a non-characteristic gritty/sandy texture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...
The Issue: HeartWare, Inc. of Miami Lakes, FL is recalling their Ventricular Assist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker XIA 3 Iliac Screwdriver Recalled by Stryker Spine Due to Surgeons...
The Issue: Surgeons have experienced unthreading of the screwdrivers outer shafts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.