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VITROS XT7600 Integrated System

FDA Recall #Z-1222-2024 — Class II — January 22, 2024

Recall #Z-1222-2024 Date: January 22, 2024 Classification: Class II Status: Ongoing

Product Description

VITROS XT7600 Integrated System

Reason for Recall

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.

Recalling Firm

Ortho-Clinical Diagnostics, Inc. — Rochester, NY

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

1,720 units (834 US, 886 OUS)

Distribution

Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Bermuda, Brazil, Canada, Chile, China, Colombia, Denmark, France, Germany, India, Italy, Japan, Mexico, Netherlands, Norway, Portugal, Russia, Singapore, Spain, Sweden, United Kingdom.

Code Information

Code Information: UDI/DI: 10758750031610; Serial Numbers: J76000109 through J76001913 (inclusive).

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.

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