Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1107-2013 — VITROS 4600 Chemistry System (VITROS 5,1 FS System family member), Product Code 6802445. Intended for use in the measurement of a variety of chemistry analytes.

U.S. FDA — Device Enforcement · United States · 2013-02-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1107-2013
Date of alert
2013-02-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ortho-Clinical Diagnostics
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
46000108
Reported risk: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on some VITROS¿ Systems may be out of its manufacturing specifications. Extension springs are part of the slide alignment guide assembly. During an internal evaluation in its manufacturing facility, it was discovered that an extension spring had insufficient force. If the extension spring does not provide sufficient force, MicroSlides may not be properly positioned within the MicroSlide incubator which has the potential to cause imprecise results. Extension springs are just one component in the slide alignment assembly. OCD's evaluation determined that the probability of an out of specification extension spring alone adversely affecting results is unlikely.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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