Reported Nov 20, 2013 · Terminated
Plum A+ Infusion Pump; List Number: 11971; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of…
Hospira Inc.
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: Hospira Inc. · 275 N Field Dr · Lake Forest, IL · 60045-2579
Is this the product you have?
- Plum A+ Infusion Pump
- List Number11971
- Product UsageThe Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
- Lot codes and dates
- List No. 11971
- Serial Numbers
2,714 of 2,714 codes
131200091312001713120018131200191312002613120028131200371312004113120042131200441312005713120058131200681312007113120074131200751312008213120096131201031312010413120107131201081312010913120115131201281312013813120143131201531312016013120164131201681312017113120174131201771312018613120187131202001312020513120220131202221312022313120226131202311312023513120237131202381312023913120247131202481312024913120251131202531312026213120270131202711312027713120279131202851312029313120294
- Amount recalled
- List No. 11971: 10,669 units
This recall covers 15 products
The agency filed one notice per product. You are reading one of them; the other 14 are below.
2 more are in the archive.
Where it was sold
Why it was recalled
Hospira has received reports of distal pressure sensor calibration drift on Plum A+ Infusers. The following error codes may be displayed during setup or infusion signifying possible calibration drift: E180/N180, E181/N181, E186/N186, E187/N187 or E346. Additionally, if the pressure sensor calibration has drifted, users may experience false distal occlusion alarms or distal occlusions that may not
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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