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 17841–17860 of 27,462 recalls
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.
Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...
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 PEEK SwiveLock Self Punching...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...
The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 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: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...
The Issue: A potential for dual-configured beds to separate or slip away from one another.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...
The Issue: A potential for dual-configured beds to separate or slip away from one another.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Medical Radrex - i Digital Radiography X-ray system Radrex-i...
The Issue: It was discovered during a procedure that when the operator made an exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex Recalled by Sysmex America Inc Due to Reported customer complaints of...
The Issue: Reported customer complaints of automated hematology analyzers catching fire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 mL Medallion¿ Syringe. Catalog Numbers: 701989001 Recalled by Merit...
The Issue: Merit Medical Systems announces a voluntary field action for the 1mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regenerex Patella RGX 3 PEG SER A PATELLA 28MM RGX Recalled by Zimmer...
The Issue: pegs shearing post-operatively
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The following systems are only affected if a Laird chiller Recalled by...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ: UNIQ FD10 722026 Recalled by Philips Electronics North America...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper Release 8.2 (Laird chiller is always installed) Recalled by...
The Issue: Due to a leak in the detector cooling system, cooling liquid may leak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wingman 35 Crossing Catheter Recalled by Medical Due to Medical is recalling...
The Issue: Medical is recalling the Wingman 35 Crossing Catheter because it may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenith Alpha Thoracic Endovascular Graft The Zenith Alpha" Thoracic...
The Issue: There have been five reports of graft thrombosis/occlusion during global...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-360 Analyzer is capable of performing two methods of immunoassay:...
The Issue: The firm has become aware of a potential issue with the AIA-360 analyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sample probes associated with: cobas 6000 Series System Recalled by Roche...
The Issue: Due to a design change in 2015, corrosion on the sample probe electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ Access Kit with Maximal Barrier Precautions for use with Recalled by...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Arterial Line Catheterization Kit The Arrow¿ Arterial...
The Issue: Arrow International initiated the recall due to reports of safety cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.