Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:115366

Plum A+ Hyperbaric Infusion Pump; List Number 11005; Labeled in part: PLUM A+ HYPERBARIC; Product Usage: 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

Official recall number

Z-0203-2014

Evidence summary

Product code
FRN
Recall status
Terminated
Event initiated
February 05, 2012
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0203-2014

Field note

Send feedback

We'll only use this to respond to your feedback.