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Terminated

Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS.

FDA Recall Z-0024-05 · Posted 2004-10-20

Recalling FirmRemel, Inc.
Recall StatusTerminated
Product CodeKZI
Date Initiated2004-09-27
Date Terminated2006-04-25
Product Quantity4,620 units (308 packages)

Reason for Recall

The product does not perform as intended with some quality control organisms (Haemophilus influenzae)

Firm Action

The recalling firm notified their customers via telephone on 9/27/04 requesting they examine their inventory and discard the recalled lot.

Root Cause

Other

Distribution Pattern

Distribution was made to medical facilities and laboratories located in IA, KS, MO, FL, NY, IL, AR, TX, and OK.

Official Source

View FDA Recall →

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

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