Web21 May 2024 · The CADD ® -Solis VIP (variable infusion profile) Ambulatory Infusion Pump is designed to facilitate patient care for a variety of adult and pediatric patients and clinical care areas. The pump can be programmed with a protocol configuration consisting of a therapy, qualifier and drug information. The pump delivers via the following delivery ... Web7 Feb 2024 · On February 2, 2024, the U.S. Food and Drug Administration (FDA) reported Smiths Medical’s recall of its CADD™ infusion system administration sets and cassette reservoirs because of tubing occlusions that may under- or not deliver medication and false no disposable attached (NDA) alarms that may prevent pump use. FDA identified it as a …
MAUDE Adverse Event Report: SMITHS MEDICAL ASD, INC. CADD …
WebSmiths Medical ASD Inc. 6000 Nathan Ln N Minneapolis MN 55442-1690: Manufacturer Reason for Recall: Smiths Medical became aware that certain Non Flow-Stop CADD(R) … WebInformation was received indicating that during use of this smiths medical cadd administration sets, under delivery was noticed. It was reported that the device use for infusion of pip-tazo. The reporter stated the iv bag had approximately 70 ml remaining at the end of scheduled infusion. The reporter stated this occurred "during the past 4-5 ... flights from las vegas to oaxaca mexico
Class 1 Device Recall CADD Disposables - accessdata.fda.gov
WebCADD ® CADD ® -Solis Infusion System The CADD-Solis Infusion System offers a modern portable design with wireless connectivity and versatility for pain management. Supported … Web17 Mar 2024 · The FDA has issued a Class I recall for Smiths Medical CADD infusion system Administration Sets and Cassette Reservoirs. The recall impacts 19,792,933 devices distributed in the U.S. from June 15, 2024 to the present. CADD ambulatory infusion systems deliver controlled amounts of medications to patients in hospital, outpatient, and home … WebRecall of CADD - SOLIS VIP AMBULATORY INFUSION PUMP According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SMITHS MEDICAL CANADA LTD. (SIMS) . What is this? A correction or removal action taken by a manufacturer to address a problem with a medical device. cher lyrics do you believe in life after love