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. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 26181–26200 of 48,219 recalls
Recalled Item: Smokehouse 220 Sweet & Spicy Barbecue Sauce Recalled by Ventura Foods, LLC...
The Issue: A plastic foreign object was inadvertently introduced into the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sysco Imperial Tartar Sauce Recalled by Ventura Foods, LLC Due to Foreign...
The Issue: A plastic foreign object was inadvertently introduced into the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sysco Imperial Glazed Hot Bacon Dressing Recalled by Ventura Foods, LLC Due...
The Issue: A plastic foreign object was inadvertently introduced into the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Health Harmony Mobile application software Product Usage: Care Innovations...
The Issue: It was discovered that in certain situations, including partial sessions and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suspension Arm (P/N: 525004 Recalled by Reliance Medical Products Inc Due to...
The Issue: Product has been found with a missing Washer, Retaining Ring, and/or Stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enoxaparin Sodium Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. A single syringe labeled as 150...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pantoprazole Sodium for Injection Recalled by AuroMedics Pharma LLC Due to...
The Issue: Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viokace (pancrelipase) tablets Recalled by ALLERGAN Due to Subpotent Drug:...
The Issue: Subpotent Drug: One lot of Viokace is being recalled since product stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Truth Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truth Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT-A-CATH II PS/Titan Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...
The Issue: A subset of Lot 7212154 A of the iChem VELOCITY Urine Chemistry strips has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Plus Recalled by Accord Media, LLC Due to Distribution of...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra Renew Recalled by Accord Media, LLC Due to Distribution of medical...
The Issue: Distribution of medical devices with unapproved green LED light used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power PORT-A-CATH II Recalled by Smiths Medical ASD Inc. Due to Certain...
The Issue: Certain models and lots of PORT A CATH implantable port kits may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CellaVision DM Software versions 6.0.1 or 6.0.2 installed on the Recalled by...
The Issue: A software malfunction was found where WBC, RBC and PLT comments added after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volumat MC Agilia Volumetric Infusion Pump Recalled by Fresenius Vial Sa Due...
The Issue: Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEKTA Digital Accelerator under the following brand names: Elekta Synergy...
The Issue: There is a potential for an uncontrolled extension of iViewGT / XVI detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee...
The Issue: Incorrect product and/or label. Sizing is labeled incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Module 3 monitoring spirometer Recalled by Mindray DS USA, Inc. dba...
The Issue: The firm made multiple changes to the product requiring the submission of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.