Remel, Inc Remel Middlebrook 7H10 Agar, Ref R01600, packaged 10 units/package. The firm name on the label is Remel, Lenexa, KS. Solid Medium recommended for use in qualitative procedures for the isolation and cultivation of mycobacteria. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Remel Middlebrook 7H10 Agar, Ref R01600, packaged 10 units/package. The firm name on the label is Remel, Lenexa, KS. Solid Medium recommended for use in qualitative procedures for the isolation and cultivation of mycobacteria.
Brand
Remel, Inc
Lot Codes / Batch Numbers
Lot 763654, Exp. 2009.07.07
Products Sold
Lot 763654, Exp. 2009.07.07
Remel, Inc is recalling Remel Middlebrook 7H10 Agar, Ref R01600, packaged 10 units/package. The firm name on the label is R due to The plate labeling is incorrect, but the outer box labeling is correct. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The plate labeling is incorrect, but the outer box labeling is correct
Recommended Action
Per FDA guidance
The recalling firm issued Important Medical Device Customer Recall Notice letters dated 5/6/08 via regular mail explaining the reason for recall and requesting all remaining inventory of the recalled lot be discarded. A Product Inventory Checklist was enclosed for completion to report the amount of inventory destroyed. A self-addressed postage-paid envelope was enclosed for return of the Product Inventory Checklist. Customers are to contact the firm's Technical Services Department at 800-447-3641 if they have inquiries concerning the letter.
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