RecallRadar

FDA Device recall Z-1221-2024

VITROS 5600 Integrated System (New and Refurbished)

On 2024-03-13 the FDA classified a Class II recall of VITROS 5600 Integrated System (New and Refurbished) by Ortho Clinical Diagnostics, citing potential For Aspiration from Unintended Sample Container During Sampling Center Processing on VITROS¿ 3600 Immunodiagnostic Systems and VITROS¿ 5600/XT 7600 Integrated Systems wh….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1221-2024
ClassificationClass II
Statusongoing
Initiated2024-01-22
Published2024-03-13
Last updated2026-09-13 11:57 UTC
CompanyOrtho Clinical Diagnostics
DistributionUS

Product

VITROS 5600 Integrated System (New and Refurbished)

Reason

Potential For Aspiration from Unintended Sample Container During Sampling Center Processing on VITROS¿ 3600 Immunodiagnostic Systems and VITROS¿ 5600/XT 7600 Integrated Systems which may lead to erroneous test results.

Identifiers

code_info
UDI/DI: (New) 10758750002740, (Refurbished) 10758750007110; Serial Numbers: J56000280, J56000330, J56000415, J56000631,…UDI/DI: (New) 10758750002740, (Refurbished) 10758750007110; Serial Numbers: J56000280, J56000330, J56000415, J56000631, J56000634, J56000721, J56000839, J56000871, J56001088, J56001209, J56001228, J56001265, J56001305, J56001355, J56001834, J56001855, J56001941, J56001998, J56002111, J56002239, J56002476, J56002492, J56002531, J56002561, J56002649, J56002655, J56002658, J56002691 and J36001164 through J36001692 (inclusive).

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1221-2024%22

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