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. 2,466 recalls have been distributed to Wyoming in the last 12 months.
Showing 17821–17840 of 27,462 recalls
Recalled Item: Dressing Shldr Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing M/U XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Back Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Recalled by Breg Inc Due to They may not have been sealed prior to...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi-Therm Hyper/Hypothermia System Recalled by Stryker Medical Division of...
The Issue: The water may reheat too quickly if the unit is in "Automatic" mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EZ-IO Needle Set 45 mm 15 ga Recalled by Teleflex Medical Due to Some...
The Issue: Some of the individual unit packaging (pouches) may be missing the lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GP161R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR GHIATAS Beaded Breast Localization Wire Recalled by Bard Peripheral...
The Issue: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GP321R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE426R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...
The Issue: Diamond particulates may break off the burr and fall into the surgical site....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...
The Issue: It was reported that a set low O2 alarm does not go off although the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...
The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.