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. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 13981–14000 of 27,462 recalls
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...
The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...
The Issue: New software version for affected ventilators reduces the probability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha with software version VA30-mobile C-arm x-ray Material # Recalled...
The Issue: Continuous operation of the Cios Alpha at high tube outputs may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...
The Issue: Kit label states not made with natural rubber latex,however safety goggles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...
The Issue: The back cover of the light head was insufficiently assembled and could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...
The Issue: The back cover of the light head was insufficiently assembled and could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton E-Pacer Recalled by Community Products, LLC Due to A design change to...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Standard Base Recalled by Community Products, LLC Due to A...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton TRAM Low Base Recalled by Community Products, LLC Due to A design...
The Issue: A design change to the load-bearing quick release buckle renders the springs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV1000 Clinical Platform Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Potential for an electrical short circuit leading to possible fire hazard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable Pump (Clinical) Recalled by Flowonix Medical Inc...
The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System" Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Anchor Tissue Retrieval System Recalled by Conmed Corporation Due to...
The Issue: Voids in the seal or a partial seal results in an open channel and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.