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

Recall Z-1404-2019 — Thio Med w/o Ind, w/Dex (10ml) 20/PK Product Usage: Recommended for use in qualitative procedures as a general purpose media for the cultivation of aerobes and anaerobes

U.S. FDA — Device Enforcement · United States · 2019-04-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1404-2019
Date of alert
2019-04-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Remel Inc
Product category
device
Product type
Devices
Reported risk: Potential for products to fail performance testing per the Instructions for Use (IFU) starting at 106 days after date of manufacturing. Expiration date is shortened from 9 months to 105 days.
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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.