Medical device recalls Moderate risk

Roche Diagnostics Operations product recalled over laceration hazard

Recall date
July 15, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Roche Diagnostics Operations, Inc. recalls URISYS 2400 Urine Analyzer Automated Urinalysis System Product Usage: The RSD 800 is a computer-controlled stand-alone…
Recall number
Z-0099-2017
FDA classification
Class II
Brand / firm
Roche Diagnostics Operations, Inc.
Sold / distributed
US Nationwide Distribution

Why it was recalled

Roche has received four reports of injury caused by the sharp edge of the center guide rail of an analyzers sample rack tray. The cleaning procedure for the sample rack tray has been revised to clarify the cleaning process.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

URISYS 2400 Urine Analyzer Automated Urinalysis System Product Usage: The RSD 800 is a computer-controlled stand-alone sorting system for sorting barcoded samples. The system has an online connection to the host.

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