Remel, Inc. ProSpecT Giardia/Cryptosporidium Microplate Assay. Catalog #: 2458496. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ProSpecT Giardia/Cryptosporidium Microplate Assay. Catalog #: 2458496.
Brand
Remel, Inc.
Lot Codes / Batch Numbers
944755
Products Sold
944755
Remel, Inc. is recalling ProSpecT Giardia/Cryptosporidium Microplate Assay. Catalog #: 2458496. due to The conjugate may cause the negative control to produce high OD readings, therefore invalidating the run.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The conjugate may cause the negative control to produce high OD readings, therefore invalidating the run.
Recommended Action
Per FDA guidance
Remel contacted each customer with a letter, by mail, requesting a count of the affected lots to be returned. Product would be replaced upon customer request.
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