Remel Thayer Martin Agar (Improved), packaged in 10-packs (Cat. #01884), 15-packs (Cat. #01885), and 100 per case (Cat.
FDA device recall Z-0069-04 · posted 2003-10-24 · Terminated
Recall details
- Recalling firm
- Remel, Inc
- Reason for recall
- Some of the product lots exhibit no growth of quality control strains of Neisseria gonorrhoeae
- Action taken
- 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
- Status
- Terminated
- Product code
- JTY
- Quantity affected
- 404/10-pks; 67/15-pks; and 33/100-pkg. cases
- Distribution
- Distribution was made nationwide to facilities with medical laboratories, including military and government facilities.
- Date initiated
- 2003-10-02
- Date posted
- 2003-10-24
- Date terminated
- 2004-02-25
- Location
- Lenexa, KS
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.