Data Foundry

Medical device recalls 2014

Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions… — Class I medical device recall Z-1482-2014

Terminated recall by Hospira Inc., reported 2014-05-07, distributed nationwide. Hospira has received customer reports of broken door assemblies on the Hospira/Abbott Acclaim Encore infusion

Recall numberZ-1482-2014
Product typeMedical device
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmHospira Inc., Lake Forest, IL, United States
Recall initiated2013-10-31
Classified2014-05-01
Reported by FDA2014-05-07
Terminated2017-08-16
DistributedNationwide (US)
Quantity13,218 infusion
Serial numbers1231453, 1231610, 12321139, 12322780, 12322801, 12322810, 12322812, 12322873, 12322878, 12322880, 12322887, 12322896, 12322903, 12322904, 12322911, 12322916, 12322917, 12322921, 12322936, 12322939, 12323056, 12323859, 12323867, 12324375, 12324767 and 2 more

Product

Abbott Acclaim 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

Hospira has received customer reports of 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-1482-2014. 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.