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

Recall Z-0792-2013 — Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the cultivation and amplification of viruses, such as respiratory viruses, enteroviruses, measles, and poliovirus from patient specimens.

U.S. FDA — Device Enforcement · United States · 2012-12-31 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0792-2013
Date of alert
2012-12-31
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Diagnostic Hybrids Inc
Product category
device
Product type
Devices
Reported risk: RhMK product fungal contamination.
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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