FDAMarch 8, 2013device

The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through the intravenous or epidural routes in a wide range of clinical settings, including ICU, CCU, SICU, trauma units, bone marrow transplant centers, burn units, oncology centers, and ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Hospira has received reports of PCA pumps not detecting distal occlusions, one of which resulted in a serious injury. The issue is caused by normal wear and tear on the Half Nut (the component/nut that travels up and down the lead screw) which prevents it from properly detecting the pressure build-up associated with a distal occlusion.

What to do

FDA enforcement status: Terminated

Brands named

hospira

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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