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. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 27381–27400 of 27,462 recalls
Recalled Item: Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage:...
The Issue: Olympus initiated a software upgrade and enhancement in 2009 and completed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 892.1650 Image-intensified fluoroscopic x-ray system Recalled by GE OEC...
The Issue: GE OEC is recalling certain 9800 Image Intensified Flouroscopic x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo Backplate Replacement CXFVR 1500 Holder The Flexible venous Reservoir...
The Issue: Backplate reservoir holders were manufactured with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroCool Breathable Impervious Surgical Gown Recalled by Kimberly-Clark...
The Issue: Complaints were received of gowns pilling or balling, linting and abrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroCool Breathable Impervious Gown with Secure Fit Surgical Recalled by...
The Issue: Complaints were received of gowns pilling or balling, linting and abrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter's elastomeric infusion pumps are non-electronic Recalled by Baxter...
The Issue: There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter's elastomeric infusion pumps are non-electronic Recalled by Baxter...
The Issue: There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter's elastomeric infusion pumps are non-electronic Recalled by Baxter...
The Issue: There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whole Body X--ray Scanner This device is indicated as a Recalled by Toshiba...
The Issue: 1. It has been found that in raw data processing for Go&Return helical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC IT3000 Recalled by GE OEC Medical Systems, Inc Due to GE Healthcare...
The Issue: GE Healthcare Surgery had discovered that using the Inverted Headset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knife Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.