Plum A+ Infusion System with Hospira MedNet List 20792-04-25 — Class II medical device recall Z-1050-2015
Terminated recall by Hospira Inc., reported 2015-02-11, distributed in NY. Plum A+ infusion system pole clamp assemblies were discovered to be cracked. If the knob on the pole clamp ass
| Recall number | Z-1050-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2014-06-11 |
| Classified | 2015-02-04 |
| Reported by FDA | 2015-02-11 |
| Terminated | 2016-11-28 |
| Distributed | NY |
| Quantity | 102 infusors |
| Reason classes | packaging |
| Serial numbers | 17737372, 17737375, 17737377, 17737378, 17737383, 17737385, 17737390, 17737394, 17737395, 17737396, 17737397, 17737398, 17737399, 17737400, 17737402, 17737405, 17737408, 17737409, 17737414, 17737416, 17737419, 17737420, 17737421, 17737422, 17737424 and 77 more |
| Model numbers | 820-95443-008 |
Product
Plum A+ Infusion System with Hospira MedNet List 20792-04-25, Pole Clamp Assembly Part Number 820-95443-008. A cassette based multi-function infusion system. Each system includes a pumping module and an assortment of disposable IV sets, optional accessories, and an operator's manual. The pole clamp assembly is used to provide a mechanism to tighten and loosen the grip of the pole clamp to remove the infuser from the IV pole.
Reason for recall
Plum A+ infusion system pole clamp assemblies were discovered to be cracked. If the knob on the pole clamp assembly is cracked, the infuser cannot be attached to the IV pole since the knob is used to tighten and loosen the grip of the pole clamp to the pole.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.