Remel, Inc. Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS.
Brand
Remel, Inc.
Lot Codes / Batch Numbers
Lot #435902, Exp. 2004-11-04
Products Sold
Lot #435902, Exp. 2004-11-04
Remel, Inc. is recalling Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The fi due to The product does not perform as intended with some quality control organisms (Haemophilus influenzae). Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product does not perform as intended with some quality control organisms (Haemophilus influenzae)
Recommended Action
Per FDA guidance
The recalling firm notified their customers via telephone on 9/27/04 requesting they examine their inventory and discard the recalled lot.
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 noticeDistribution
As reported by FDA
AR, FL, IL, IN, IA, KS, MO, NY, OK, TX
Page updated: Jan 10, 2026