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. 2,510 recalls have been distributed to Wyoming in the last 12 months.
Showing 13481–13500 of 27,462 recalls
Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: There has been an increase in complaints related to leaks, suction issues,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTec Neonatal Starter Set with and without Service Gas (2 Recalled by...
The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTec Membrane Changer Set (1 charger plus 1 insert) - Recalled by SenTec...
The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: There has been an increase in complaints related to leaks, suction issues,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: There has been an increase in complaints related to leaks, suction issues,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: There has been an increase in complaints related to leaks, suction issues,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTec Membrane Changer Insert [5 pcs - Product Usage: is Recalled by SenTec...
The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: There has been an increase in complaints related to leaks, suction issues,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revive Reusable Bladder Support Recalled by Rinovum Women's Health Due to...
The Issue: The product is unable to meet the use life of 31 cycles and may split or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401 Recalled by Oakworks Inc Due...
The Issue: Table assembly error with incorrect actuators for the lateral and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...
The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and...
The Issue: The 0-arm 1000 Imaging System uses energy from the batteries to generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Item code: 8881200029 Recalled by...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.