The Plum A+3 Infusion System is a cassette based multifunction… — Class II medical device recall Z-0288-2014
Terminated recall by Hospira Inc., reported 2013-11-20, distributed nationwide. Plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure
| Recall number | Z-0288-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2013-02-01 |
| Classified | 2013-11-14 |
| Reported by FDA | 2013-11-20 |
| Terminated | 2016-12-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | CR, DO |
| Quantity | 7,692 units |
| Reason classes | device malfunction |
| Serial numbers | 14040001, 14040002, 14040003, 14040004, 14040005, 14040006, 14040008, 14040009, 14040010, 14040011, 14040012, 14040014, 14040015, 14040016, 14040017, 14040018, 14040019, 14040020, 14040021, 14040022, 14040023, 14040024, 14040025, 14040026, 14040027 and 475 more |
Product
The Plum A+3 Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+3 Infusion System is designed to deliver parenteral, enteral, or epidural infusions over a broad range of infusion rates from multiple fluid container types. The Plum A+3 Infusion System includes an infuser, disposable IV sets (hereafter called a set), optional accessories, and this operator's manual. The Plum A+ Infusion System with Hospira MedNet Software is indicated for use in parenteral, enteral and epidural therapies and the administration of whole blood and blood products.
Reason for recall
Plum A+ infusers have the potential for the distal (occlusion) press sensor pin to break. The distal pressure sensor pin is a part of the overall subsystem that measures the pressure within the distal line of the administration set and indicates the presence of a full or partial distal occlusion. A broken distal pin can only be detected via a visual inspection of the distal pressure pin. A broken
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0288-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.