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

Recall Z-0269-2020 — VITROS chemistry Products K+ Slides, Catalog No. 8157596. MicroSlides which contain reagents in a dry, multi-layered form.

U.S. FDA — Device Enforcement · United States · 2019-09-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0269-2020
Date of alert
2019-09-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ortho-Clinical Diagnostics
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
410209876551
Reported risk: Users may experience intermittent slide dispense issues with some cartridges due to the anti-backup platen failing to advance inside the cartridge.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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