BD Diagnostic Systems BD, Proteus OX19 Antigen Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD, Proteus OX19 Antigen
Brand
BD Diagnostic Systems
Lot Codes / Batch Numbers
Catalogue #240782, Lot #3035884
Products Sold
Catalogue #240782, Lot #3035884
BD Diagnostic Systems is recalling BD, Proteus OX19 Antigen due to Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instruct. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Febrile Antigens and Control Antisera that were released prior to August 2003 contained the 12/2000 revised insert that had incorrect testing instructions.
Recommended Action
Per FDA guidance
Consignees were notified by letter beginning 10/20/2004.
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