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: Glendale Personal Injury LawyerFDA Anounces Class 1 Recall of Infusion Pump
By Greg Owen
The most serious type of FDA recall is known as a "Class I recall." This type of recall is only issued if a given defective medical device will cause serious injury or death. According to the FDA recall notice, Medtronic notified its customers of the SynchroMed El Implantable Infusion Pump via a letter dated August 3, 2007.
The Implantable Infusion Pump administers drugs to a specific site in the body to treat pain, spasticity (continuous muscle contraction), and cancer. The Infusion Pump recall involved models 8626-10, 8626L-10, 8626-18, 8626L-18, 8627-10, 8627L-10, 8627-18, and 8627L-18. Only those models with motors manufactured before September 1999 are affected by the recall.
Full post as published by Glendale Personal Injury Lawyer on February 11, 2008 (boomark / email).
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