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. 2,404 recalls have been distributed to Wyoming in the last 12 months.
Showing 21021–21040 of 27,462 recalls
Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...
The Issue: Cracks were discovered in the PET tray of a small population of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid...
The Issue: Some devices exhibit backup VVI operation due to a backup reset.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....
The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...
The Issue: patient procedure interruption due to a potential system failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...
The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: The Centricity...
The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...
The Issue: DLS pin breakage during planned implant removal, after uneventful and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LX3 Floor Stand for Endure Luxite Envision Optical System Recalled by Alcon...
The Issue: Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: The Centricity Universal Viewer...
The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fundus Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medium -Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cadiere Forceps Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fenestrated Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maryland Dissector Recalled by Intuitive Surgical, Inc. Due to In certain...
The Issue: In certain circumstances involving select da Vinci Si Single-Site...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.