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Terminated

Remel Thayer Martin Agar (Improved), packaged in 10-packs (Cat. #01884), 15-packs (Cat. #01885), and 100 per case (Cat. #01886). The responsible firm on the label is Remel, Lenexa, KS.

FDA Recall Z-0069-04 · Posted 2003-10-24

Recalling FirmRemel, Inc
Recall StatusTerminated
Product CodeJTY
Date Initiated2003-10-02
Date Terminated2004-02-25
Product Quantity404/10-pks; 67/15-pks; and 33/100-pkg. cases

Reason for Recall

Some of the product lots exhibit no growth of quality control strains of Neisseria gonorrhoeae

Firm Action

The recalling firm initiated recall via letter dated 10/2/03 issued regular mail requesting the customer destroy remaining inventory of the affected lot numbers.

Root Cause

Other

Distribution Pattern

Distribution was made nationwide to facilities with medical laboratories, including military and government facilities.

Official Source

View FDA Recall →

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

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