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Terminated

CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.

FDA Recall Z-0209-2018 · Posted None

Recalling FirmRemel Inc
Recall StatusTerminated
Product CodeJTZ
Date Initiated2017-11-02
Date Terminated2020-08-05
Product Quantity7 units

Reason for Recall

Product may have incorrect cation information detailed on the product label.

Firm Action

The recalling firm issued letters dated 11/2/2017 via regular mail on 11/2/2017 notifying the customer of the incorrect labeling information and providing them the correct labeling information.

Root Cause

Under Investigation by firm

Distribution Pattern

Distribution was made to AL, MD, ME, NC, and TN. There was no foreign/military/government distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K802498MUELLER HINTON AGAROxoid U.S.A., Inc. · 1980-11-12

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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