FDA Device recall Z-1483-2014

Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell components and entera…

FDA Device
Class I
terminated
Published 2014-05-07

On 2014-05-07 the FDA classified a Class I recall of Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell components and entera… by Hospira, citing 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 oc….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1483-2014
Classification	Class I
Status	terminated
Initiated	2013-10-31
Published	2014-05-07
Last updated	2026-09-13 11:53 UTC
Company	Hospira
Distribution	US

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

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.

Identifiers

code_info	List Number: 12237; Serial Numbers: 12670196, 12670182, 12670203, 12670281, 12671061, 12671058, 12671175, 1271… List Number: 12237; Serial Numbers: 12670196, 12670182, 12670203, 12670281, 12671061, 12671058, 12671175, 12718477, 12672450, 12672413, 12716099, 12716071, 12671563, 12672061, 12672079, 12672156, 12718948, 12717835, 12716259, 12716268, 12671580, 12671554, 12716244, 12716293, 12671647 , 12672014 , 12672021 , 12672064 , 12672074 , 12672137 , 12672138 , 12672143 , 12672173 , 12672179 , 12672185 , 12672186 , 12672161 , 12672217 , 12716140 , 12716324 , 12716396 , 12716489 , 12716316 , 12671666 , 12672065 , 12672175 , 12716251 , 12716550 , 12716398 , 12716963 , 12716451 , 12716345 , 12716519 , 12716693 , 12716477 , 12716610 , 12716638 , 12716344 , 12716538 , 12716515 , 12716315 , 12716720 , 12716623 , 12716787 , 12716822 , 12717186 , 12716738 , 12717343 , 12716798 , 12716812 , 12716532 , 12717123 , 12716849 , 12717281 , 12717049 , 12717160 , 12717359 , 12717028 , 12717298 , 12673508 , 12673609 , 12673114 , 12

code_info

List Number: 12237; Serial Numbers: 12670196, 12670182, 12670203, 12670281, 12671061, 12671058, 12671175, 1271…

List Number: 12237; Serial Numbers: 12670196, 12670182, 12670203, 12670281, 12671061, 12671058, 12671175, 12718477, 12672450, 12672413, 12716099, 12716071, 12671563, 12672061, 12672079, 12672156, 12718948, 12717835, 12716259, 12716268, 12671580, 12671554, 12716244, 12716293, 12671647 , 12672014 , 12672021 , 12672064 , 12672074 , 12672137 , 12672138 , 12672143 , 12672173 , 12672179 , 12672185 , 12672186 , 12672161 , 12672217 , 12716140 , 12716324 , 12716396 , 12716489 , 12716316 , 12671666 , 12672065 , 12672175 , 12716251 , 12716550 , 12716398 , 12716963 , 12716451 , 12716345 , 12716519 , 12716693 , 12716477 , 12716610 , 12716638 , 12716344 , 12716538 , 12716515 , 12716315 , 12716720 , 12716623 , 12716787 , 12716822 , 12717186 , 12716738 , 12717343 , 12716798 , 12716812 , 12716532 , 12717123 , 12716849 , 12717281 , 12717049 , 12717160 , 12717359 , 12717028 , 12717298 , 12673508 , 12673609 , 12673114 , 12

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1483-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.