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. 2,342 recalls have been distributed to Wyoming in the last 12 months.
Showing 35221–35240 of 48,219 recalls
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: 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: 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 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: Crocodile 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: 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.
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: CDI 500 Blood Parameter Monitoring System. Provides continuous Recalled by...
The Issue: Inaccuracies in SvO2, temperature, pH, pCO2, pO2, Hematocrit, and Potassium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a...
The Issue: Software defect that impacts image alignment when using the automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Vascular Loop Catalog Number CH111 Recalled by International Biophysics...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Recalled by...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBC Aortic Punch Catalog Numbers APM40 Recalled by International Biophysics...
The Issue: It was discovered that the heat seal placed onto sterile pouches may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KABOOM action strips Recalled by Blue Square Market, Inc. Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG) Recalled by Blue...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared Sibutramine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.