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

Recall Z-1400-2017 — Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,

U.S. FDA — Device Enforcement · United States · 2017-02-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1400-2017
Date of alert
2017-02-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Remel Inc
Product category
device
Product type
Devices
Reported risk: Test organisms exhibit poor growth when grown using the test agar. The poor growth can give users incorrect AST zones when performing susceptibility tests.
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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