Reported Jul 19, 2017 · Terminated
The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies…
Icu
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: ICU · 600 N Field Dr · Lake Forest, IL · 60045-4835
Is this the product you have?
- The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.
- Lot codes and dates
- List number20679 Serial Number
3,257 of 3,257 codes
154410191544102015441037154410441544108215441093154411181544122615441229154412301544124015441241154412441544124615441247154412491544125315441256154412581544126015441265154412661544127015441271154412721544127515441285154413031544130415441315154413181544132115441323154413251544134915441350154413671544136915441371154413721544137815441395154413991544140515441409154414111544143715441458154414891544149215441493154415021544150615441508154415131544151515441516154415201544152215441524
- List number20679 Serial Number
- Amount recalled
- 7351 units
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
- Nationwide
Why it was recalled
A possible interruption of therapy when an E321 error code occurs while using the infuser, which is caused by battery issues.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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