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. 1,800 recalls have been distributed to Wyoming in the last 12 months.
Showing 30341–30360 of 48,219 recalls
Recalled Item: KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol...
The Issue: Failed Stability Specifications: Low Out of Specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simply Nature Organic Red Split Lentils Recalled by Aldi Inc Due to...
The Issue: Product may contain undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Simply Nature Organic Green Lentils Recalled by Aldi Inc Due to Undeclared Wheat
The Issue: Product may contain undeclared wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Life Rising TT Side Head Regulator Recalled by Life Rising Corp S Due to...
The Issue: High levels of lead discovered in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nabisco Oreo Fudge Creme Original Variety Recalled by Mondelez International...
The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nabisco Oreo Fudge Creme Mint Variety Recalled by Mondelez International Due...
The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage:...
The Issue: IBA is initiating this recall to address an issue identified with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S...
The Issue: A change in the calibration curve causing an increase in false prozone flags.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gomco Circumcision Clamps with separate O-Ring Component: The device is...
The Issue: Aesculap has received complaints of excessive bleeding after use of Gomco...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...
The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....
The Issue: Breach in sterile barrier compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...
The Issue: Failed Dissolution Specifications: The firm was notified that there was a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXI NOZZLE SHORT Product Usage: These products are used for Recalled by...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA MADgic Recalled by Teleflex Medical Due to Product Defect; These...
The Issue: Product Defect; These products may produce a straight stream instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CRP Slides: 1) VITROS¿ Chemistry Products CRP Slides (250 Recalled by...
The Issue: CRP samples diluted using VITROS Chemistry Products Specialty Diluent,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.