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. 2,531 recalls have been distributed to Wyoming in the last 12 months.
Showing 9281–9300 of 27,462 recalls
Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien HysteroLux Fluid Management System Control Unit Recalled by WOM...
The Issue: When the display of inflow volume to the uterus reaches 32450 ml, the fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in...
The Issue: Out of Specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and...
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10....
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Gentherm Medical, LLC...
The Issue: There is a potential risk of device contamination and patient infection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argyle UVC Insertion Tray containing Safety Scalpel N11 (vendor part...
The Issue: The current Argyle UVC Insertion Tray does not include a specific IFU to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235- designed to produce and deliver a proton beam Recalled by Ion...
The Issue: Users may be misled by the popup message displayed by the Proton Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized,...
The Issue: Not properly sterilized, because the outer pouch seal on the Tyvek header...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to The polyester-based...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP A 40 Recalled by Philips Respironics, Inc. Due to The...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP Hybrid A30 (not marketed in US) Recalled by Philips...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arjo Citadel beds originally assembled with the IndiGo modules during...
The Issue: The IndiGo power cord might wear during use which could lead to its damage,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for 15%...
The Issue: There is a potential for 15% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for >10%...
The Issue: There is a potential for >10% under-recovery on Activated Alanine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 3D Imaging Recalled by GE OEC Medical Systems, Inc Due to There is a...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Recalled by...
The Issue: Due to a design issue, inflation syringe handle separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite mobile C-arm - Product Usage: intended to provide Recalled by GE...
The Issue: There is a potential that the coin cell battery used to monitor X-Ray tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.