Dade Behring Inc. Dade Fibrin(ogen) Degradation Products (FDP) Detection Set. Catalog number B4233-10E Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dade Fibrin(ogen) Degradation Products (FDP) Detection Set. Catalog number B4233-10E
Brand
Dade Behring Inc.
Lot Codes / Batch Numbers
Lot number P152010 exp 4/30/06.
Products Sold
Lot number P152010 exp 4/30/06.
Dade Behring Inc. is recalling Dade Fibrin(ogen) Degradation Products (FDP) Detection Set. Catalog number B4233-10E due to positive control shows weak agglutination reaction. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
positive control shows weak agglutination reaction
Recommended Action
Per FDA guidance
The recalling firm notified their customers on 6/21/05 via letter dated 6/17/05. The customers were instructed to discontinue the use of the affected lot and discard any remaining inventory.
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