FDAJanuary 16, 2015device
BodyGuard 323 pump, models 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, 100-603XSA and 100-603XSAP
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due to the potential for an over delivery.
What to do
FDA enforcement status: Terminated
Brands named
cme americacme
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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