Reported Feb 25, 2015 · Terminated
BodyGuard 323 pump, models 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, 100-603XSA and 100-603XSAP
CME America, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CME America, LLC · 14998 W 6th Ave · Golden, CO · 80401-6587
Is this the product you have?
BodyGuard 323 pumpmodels 100-510PXSI100-516PXS100-517PXS100-518PXS100-603XSA and 100-603XSAP
- Lot codes and dates
- All product with USA36A4.4 version of software affected
- Amount recalled
- 3,186
Where it was sold
- Nationwide
- VA
Why it was recalled
CME America is recalling the BodyGuard and BodyGuard 323 Infusion pumps due to the potential for an over delivery.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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