Remel Inc Remel RapID Inoculation Fluid, Microorganism differentiation and identification device, Packaged in 1-ml tube, Catalog Number: R8325102, 20/pack, Remel, Lenexa, KS 66215 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Remel RapID Inoculation Fluid, Microorganism differentiation and identification device, Packaged in 1-ml tube, Catalog Number: R8325102, 20/pack, Remel, Lenexa, KS 66215
Brand
Remel Inc
Lot Codes / Batch Numbers
Lot 518113
Products Sold
Lot 518113
Remel Inc is recalling Remel RapID Inoculation Fluid, Microorganism differentiation and identification device, Packaged in due to Failure to produce reaction: Use of the product with various RapID Identification systems panels may exhibit poor or no reactions.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Failure to produce reaction: Use of the product with various RapID Identification systems panels may exhibit poor or no reactions.
Recommended Action
Per FDA guidance
Consignees were notified by an Important Medical Device Customer Advisory Notice on 10/23/07. The letter instructs users to review inventory and discard any affected products. The letter also instructs users to return a product inventory checklist by 11/23/07. For additional information, contact 1-800-447-3641.
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