Remel, Inc 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. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Remel, Inc
Lot Codes / Batch Numbers
10 pack - Lot #384341, Exp. 11/03/2003, 15 pack - Lot #384342, Exp. 11/3/2003, 100/cs - Lot #384343
Products Sold
10 pack - Lot #384341, Exp. 11/03/2003; 15 pack - Lot #384342, Exp. 11/3/2003; 100/cs - Lot #384343
Remel, Inc is recalling Remel Thayer Martin Agar (Improved), packaged in 10-packs (Cat. #01884), 15-packs (Cat. #01885), and due to Some of the product lots exhibit no growth of quality control strains of Neisseria gonorrhoeae. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some of the product lots exhibit no growth of quality control strains of Neisseria gonorrhoeae
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026