Reported Sep 14, 2016 · Terminated
Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum A+ Infusion Systems are a multi-purpose family of devices…
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+ Hyperbaric Infusion Pump. List Number 11005. The Plum A+ Infusion Systems are a multi-purpose 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.
- Lot codes and dates
- List Number 11005
- Serial numbers
179 of 179 codes
167922011679220216792205167922061679220816792209167922101679221116792213167922161679221716792219167922201679222216792223167922241679222516792226167922271679222816792230167922321679223316792234167922351679223616792238167922391679224016792241167922421679224416792245167922461679224816792249167922501679225116792252167922531679225416792255167922561679225716792258167922591679226016792261167922631679226416792265167922661679226816792269167922711679227216792273188074021880740518807406
- Amount recalled
- 357,778 total
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
- PR
Why it was recalled
The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized, possibly resulting in alarms and delay or interruption of therapy.
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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