Am J Health Syst Pharm. 2006;63(16):1528-1538. We report anticipated failure modes that occurred postimplementation despite the implementation of our recommended actions. Most of the listed failures ...
Iradimed Corporation announced that it has received FDA 510(k) clearance for its next-generation MRidium® 3870 IV Infusion Pump System, making it the only supplier of non-magnetic MRI-compatible ...
STATEN ISLAND, N.Y. -- Despite a nationwide recall, Staten Island University Hospital’s parent company is continuing the use of possibly defective IV equipment, according to a document obtained by the ...
A multidisciplinary team was assembled to perform an FMEA of the i.v. medication administration process incorporating pump technology and to report its findings to the hospital performance-improvement ...
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