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. 1,077 recalls have been distributed to Wyoming in the last 12 months.
Showing 3941–3960 of 27,462 recalls
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T- Magnetic Resonance (MR) systems are Recalled...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Model Number (REF): (1) 782105 (2) 781271 Recalled by...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marlin 1.5T - Magnetic Resonance (MR) systems are Medical Electrical...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T for PET -Magnetic Resonance (MR) systems are Medical Recalled...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Cerene Cryotherapy Device Product Name: DEVICE Recalled by...
The Issue: Error code 003 was not listed in certain rows of the Device Instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T- Magnetic Resonance (MR) systems are Medical Electrical Systems...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Model Number (REF): (1) 782140 Recalled by Philips North...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Model Number (REF): (1) 781345 Recalled by Philips North...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Initial system Model Number (REF): 781178 Recalled by Philips...
The Issue: The g-MDU (global Mains Distribution Unit) L3 terminal connection may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.