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

Recall Z-2126-2013 — Microscan plus Negative Breakpoint Combo 4 Sold outside of US only. Product Usage: MicroScan¿ Synergies plus¿ Panels & MicroScan¿ Rapids plus (Negative) - For use in determining quantitative and/or qualitative antimicrobial agent susceptibility and/or identification for gram-negative bact

U.S. FDA — Device Enforcement · United States · 2013-08-21 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2126-2013
Date of alert: 2013-08-21
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Siemens Healthcare Diagnostics, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10460272

Reported risk: Confirmed increase in false susceptible and false intermediate misreads for Imipenem and/or meropenum on Synergies plus Negative and rap ID/S plus Negative panels read on Walk Away System.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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