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

Recall Z-1093-2017 — Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50Kg sizes

U.S. FDA — Device Enforcement · United States · 2016-04-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1093-2017
Date of alert
2016-04-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Acumedia Manufacturers, Inc.
Product category
device
Product type
Devices
Reported risk: light precipitate may form in prepared plates of Acumedia Tryptic Soy Agar (7100) Lot# 108166. While there is no change in growth performance of this medium, the formation of particulate matter may be misinterpreted as growth in poured plates thereby leading to inaccurate counts.
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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