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infusion pump Blogs and DiscussionsArticles

 
Class I Medical Device Recall: Hospira Inc., Abbott Acclaim Infusion Pumps and Hospira Acclaim Encore Infusion Pumps - Broken Do by FDA Hospira received customer reports of broken door assemblies on the Abbott Acclaim infusion pumps and the Hospira Acclaim Encore infusion pumps. When the door is closed properly, it helps ensure that the tubing
Medtronic Drug Infusion Pumps: Recall - Intermittent or Permanent Pump Motor Stall by FDA that using unapproved drugs with the SynchroMed Infusion Pump may negatively impact the pump’s performance. The use of unapproved drugs can lead to intermittent or permanent pump motor stall and cessation of drug infusion...
WalkMed Infusion Issues Nationwide Recall of Triton Infusion Pump by FDA , Colorado, is initiating a nationwide recall of a total of 2018 Triton Pole Mount Infusion Pumps. The pumps have been found to possibly have a problem with the pump door open alarm, which potentially could result in over infusion...
Sigma Spectrum Infusion Pump Model 35700: Class 1 Recall: Risk of Over-Infusion by FDA professionals of the class 1 recall of the SIGMA Spectrum Infusion Pump Model 35700.  These units may fail... healthcare facilities to verify whether the serial numbers for their infusion pumps fall within the range...
MedStream Programmable Infusion Pump and Refill Kits by Codman and Shurtleff: Class 1 Recall - Drug Over Infusion by FDA (bradycardia), loss of consciousness, and/or death. BACKGROUND: The MedStream Programmable Infusion Pump.... Report any malfunctions or adverse events related to the MedStream Programmable Infusion Pumps and refill...
WalkMed Infusion Issues Nationwide Recall of Triton Pole Mount Infusion Pumps by FDA Pole Mount Infusion Pumps. The reason for this recall is that the pump door open alarm does not... injury or death. Consumers who have Triton Pole Mount Infusion Pumps which are being recalled...
Class I Medical Device Recall: Codman and Shurtleff MedStream Programmable Infusion Pump and Refill Kits - Drug Over Infusion by FDA The MedStream Programmable Infusion Pump is an implanted drug delivery system used in the US for the chronic delivery of Baclofen to treat muscle symptoms and used in Europe, Middle East, and Africa (EMEA
Infusion Pump Recall For Baxter – Will Offer Exchange Sigma Spectrum for Recalled Colleague Models by Medical Quack Patient ExpertHealth Maven today announced that it will recall COLLEAGUE infusion pumps from the U.S. market pursuant to an order... under which the company has been pursuing remediation of the infusion pumps. The decree permits FDA to require the recall...
Update: FDA Orders Baxter to Recall Infusion Pumps – Not Meeting Timeline – Bar Code Tags Would Make Compliance Eas by Medical Quack Patient ExpertHealth Maven Monday, May 3, 2010 Infusion Pump Recall For Baxter – Will Offer Exchange Sigma Spectrum... remediation of the infusion pumps. The decree permits FDA to require the recall of the pumps, and FDA...
Infusion Pumps: Making Medical Technology Foolproof by Jamie C. Patient Expert Millions of infusion pumps are used in hospitals, nursing facilities and homes. The pumps... with an infusion pump is reported to the Federal Food and Drug Administration, which happens more than 11,000 times...

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Treatment ... e severe allergic reactions in some people. This is known as an infusion reaction and can be potentially fatal if left untreated ... » Read on
Treatment ... e severe allergic reactions in some people. This is known as an infusion reaction and can be potentially fatal if left untreated ... » Read on