Recall reason: According to information on the FDA recall page, the agency received "reports about the presence of particulate matter and the potential absence of filter membrane layers int eh filter set . . . [this] may contaminate a solution. This could result in bloodstream infections that may cause fever, septic shock, multiple organ dysfunction, and other serious adverse health consequences including death."
When recall was initiated: August 24, 2016
Number of U.S. units impacted: 130,100 units
For more information, visit the FDA Recall page.
[Image courtesy of FDA RECALL PAGE]
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