WebThe BodyGuard 121 dual-channel ambulatory electronic infusion pump can deliver … WebApr 27, 2024 · CMEAmerica BodyGuard ® Microset Infusion Set Recall Details. On Sept. 16, 2024, the company initiated a voluntary recall to notify customers that certain lots of BodyGuard ® Microset infusion sets, when used with the BodyGuard ® infusion pump, may under-deliver fluids up to 50% at the highest flow rates. At the time of the recall, …
CME America Provides Update on Two Previously …
WebJan 7, 2024 · 303-936-4945. Manufacturer Reason. for Recall. Infusion Pump Systems may have a delivery inaccuracy of up to 13%, which may result in 1) faster than expected drug delivery when infusing at a very low rate (0.1 mL/h), or 2) slower than expected drug delivery when infusing at high flow rates (greater-than 500 mL/h) FDA Determined. WebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). knott properties maryland
B.Braun and CME America Partner To Provide BodyGuard® …
WebAug 5, 2024 · The BodyGuard Infusion Pump System delivers fluids and medications … WebThe CME BodyGuard 121 Infusion Pump is no longer cleared for use in the United States and has been removed from the market. Check out our inventory for current infusion pumps on the market. The CME … WebBodyGuard 323 Infusion Pump System Operator Manual 0473 Manufacturer: USA Headquarters: Caesarea Medical Electronics Ltd. CME America, LLC ... www.cme-infusion.com 877-263-0111 Email: [email protected] EDITION March 2009 Ref.: 100-090XC . BodyGuard Operator Manual ... red gold coin