Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral… — Class I medical device recall Z-1483-2014
Terminated recall by Hospira Inc., reported 2014-05-07, distributed nationwide. Broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps. If the door assembly breaks, it ma
| Recall number | Z-1483-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hospira Inc., Lake Forest, IL, United States |
| Recall initiated | 2013-10-31 |
| Classified | 2014-05-01 |
| Reported by FDA | 2014-05-07 |
| Terminated | 2017-08-16 |
| Distributed | Nationwide (US) |
| Quantity | 13,218 infusion |
| Serial numbers | 12670004, 12670006, 12670013, 12670026, 12670032, 12670038, 12670040, 12670043, 12670046, 12670049, 12670051, 12670062, 12670064, 12670066, 12670069, 12670075, 12670080, 12670082, 12670086, 12670090, 12670093, 12670106, 12670152, 12670157, 12670166 and 475 more |
Product
Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell components and enteral fluids using a wide variety of standard administration sets and fluid containers.
Reason for recall
Broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps. If the door assembly breaks, it may prevent the door from closing properly and unrestricted flow may occur. If the door cannot be closed, the pump cannot be used which can result in a delay in therapy.
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-1483-2014. 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.