Reported Sep 28, 2016 · Terminated
LifeCare PCA 3, PCA Serial List Number 12384 Allows for clinician administration or self-administration of analgesic…
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?
- LifeCare PCA 3, PCA Serial List Number 12384 Allows for clinician administration or self-administration of analgesic medications.
- Lot codes and dates
- Serial Number
69 of 69 codes
129212041292297612924008129258611292592412925998129285281292880712929016129291261292043212920820129208561292091512921404129214131292230412922976129258611292599812927215129290161293104412931141129311551293119212931244129313421293136112931413129316101293163912931649129319111292148012921487129237231292432612924350129245461292525912925447129263151292793812928075129286141293041812930709129308901293144112931760129319111293248712932717129207541292079112920897129210631292161312922062
- Serial Number
- Amount recalled
- 69
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Screw rotation error occurring when the pump detects a mismatch between the number of steps given to the motor driving delivery and the number of steps the motor actually took. When this malfunction occurs, the pump will alarm and infusion stops.
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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