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. 2,378 recalls have been distributed to Wyoming in the last 12 months.
Showing 24621–24640 of 48,219 recalls
Recalled Item: Superfood Salad Kit - 6.8 lbs. - sold to Kroger Recalled by Papa John's...
The Issue: It was discovered that a bulk salad kit was produced using the wrong...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A nonsterile bulk product designated for further processing in a tray was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Admelog Solostar (insulin lispro injection) Recalled by Sanofi-Aventis U.S....
The Issue: Temperature Abuse: Product samples of Admelog may not have been shipped at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc...
The Issue: Incorrect Product Formulation: wrong sunscreen product in the package.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities and Degradation Specifications and Subpotent Drug:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by Medgyn Products, Inc. Due...
The Issue: CGMP Deviations: The manufacturer of this product recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AbViser AutoValve IAP (intra- abdominal pressure) Monitoring Device Recalled...
The Issue: Bubble Leak Testing on AbViser AutoValve IAP Monitoring Devices without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...
The Issue: Incorrect expiration being entered for one lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...
The Issue: The analyzer software may cause a mis-match of patient demographics and test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Powder Free Vinyl Exam Gloves Recalled by Cypress Medical Products LLC Due...
The Issue: The firm is recalling one lot of McKesson Powder Free Vinyl Exam Gloves...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Waterpik Sonic-Fusion Professional Recalled by Water Pik, Inc. Due to...
The Issue: Charging base may overheat with localized melting and sparking, possibly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.