FDA Device recall Z-2362-2015

Alaris Syringe Pump, Model No. 8110

FDA Device
Class I
terminated
Published 2015-08-26

On 2015-08-26 the FDA classified a Class I recall of Alaris Syringe Pump, Model No. 8110 by Carefusion 303, citing channel Error code is displayed on the PC unit with an audio and visual alarm, and on the syringe module. After the error is cleared on the PCU, the syringe pump is unresponsive t….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2362-2015
Classification	Class I
Status	terminated
Initiated	2015-07-21
Published	2015-08-26
Last updated	2026-09-13 11:53 UTC
Company	Carefusion 303
Distribution	US

Product

Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

Reason

Channel Error code is displayed on the PC unit with an audio and visual alarm, and on the syringe module. After the error is cleared on the PCU, the syringe pump is unresponsive to key presses until the next power cycle, or the module is detached and reattached.

Identifiers

code_info	4051531 4051532 4051533 4051534 4051535 4051684 4051685 4051686 4051687 4051688 4051689 4051690 4051691 40… 4051531 4051532 4051533 4051534 4051535 4051684 4051685 4051686 4051687 4051688 4051689 4051690 4051691 4052487 4052488 4052489 4052490 4052492 4052493 4052495 4052497 4052499 4052500 4052501 4052502 4052503 4052504 4052505 4052507 4052509 4052510 4053437 4053547 4055907 4059581 4052494 4052496 4052508 4052511 4052491 4052498 4048982 4048983 4048985 4048986 4048987 4048988 4048990 4048991 4048992 4048993 4048994 4048995 4048996 4048997 4048999 4049000 4049002 4049231 4049232 4049233 4049234 4049236 4049237 4049238 4049239 4049241 4049242 4049243 4049244 4049245 4049246 4049248 4049250 4049251 4049252 4049253 4049255 4049256 4049257 4049989 4049990 4049991 4049993 4049994 4049996 4049997 4049998 4050000 4050001 4050002 4050003 4050004 4050005 4050006 4050008 4050010 4050011 4050012 4050013 4050449 4050450 4050451 4050452 4050453 4050454 4050456 4050457 4050458 4050459 4050460 4

code_info

4051531 4051532 4051533 4051534 4051535 4051684 4051685 4051686 4051687 4051688 4051689 4051690 4051691 40…

4051531 4051532 4051533 4051534 4051535 4051684 4051685 4051686 4051687 4051688 4051689 4051690 4051691 4052487 4052488 4052489 4052490 4052492 4052493 4052495 4052497 4052499 4052500 4052501 4052502 4052503 4052504 4052505 4052507 4052509 4052510 4053437 4053547 4055907 4059581 4052494 4052496 4052508 4052511 4052491 4052498 4048982 4048983 4048985 4048986 4048987 4048988 4048990 4048991 4048992 4048993 4048994 4048995 4048996 4048997 4048999 4049000 4049002 4049231 4049232 4049233 4049234 4049236 4049237 4049238 4049239 4049241 4049242 4049243 4049244 4049245 4049246 4049248 4049250 4049251 4049252 4049253 4049255 4049256 4049257 4049989 4049990 4049991 4049993 4049994 4049996 4049997 4049998 4050000 4050001 4050002 4050003 4050004 4050005 4050006 4050008 4050010 4050011 4050012 4050013 4050449 4050450 4050451 4050452 4050453 4050454 4050456 4050457 4050458 4050459 4050460 4

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-2362-2015%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.