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. 2,535 recalls have been distributed to Wyoming in the last 12 months.
Showing 7601–7620 of 27,462 recalls
Recalled Item: BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site Recalled by...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Flow Controller Extension Set with Needleless Y-Site Recalled by...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Randox Serology I Positive Control contains the following analytes...
The Issue: ***Update** :HBsAg analyte is also Non-Reactive on the Ortho Vitros analyser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Extension Set with 2 Needleless Y-Site Recalled by CAREFUSION...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Extension Set with 4-way stopcock Recalled by CAREFUSION Due to...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MaxGuard Extension Set Recalled by CAREFUSION Due to Administration set,...
The Issue: Administration set, and extension set product labels list expiration year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 IN (17 cm) APPX 0.78 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroClave Clear Neutral Connector Recalled by ICU Medical, Inc. Due to Due...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" (15 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroClave Clear Neutral Connector. A bidirectional connector used as an...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8.5" (22 cm) Appx 0.85 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5" (17 cm) Appx 0.84 ml Recalled by ICU Medical, Inc. Due to Due to a...
The Issue: Due to a manufacturing defect which results in a visible gap between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kits: Single Pigtail Catalog Number: 6501...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Transbronchial Aspiration Needle Catalog Number: 4621 Recalled by...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.