Becton Dickinson Medical Systems CRITIFLO(tm) flush kit. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CRITIFLO(tm) flush kit.
Brand
Becton Dickinson Medical Systems
Lot Codes / Batch Numbers
Part Number 687198, Lot Numbers 301850, 302267, 303012, 305055.
Products Sold
Part Number 687198, Lot Numbers 301850, 302267, 303012, 305055.
Becton Dickinson Medical Systems is recalling CRITIFLO(tm) flush kit. due to Device could permit an over-infusion of IV solutions during pressure monitoring procedures.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Device could permit an over-infusion of IV solutions during pressure monitoring procedures.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 8/22/2005 and told to immediately locate and quarantine all affected product for return to BD. Customer Recall Response Card was to completed and returned. For questions concerning the recall, call 800-453-4538 between 8AM and 5PM MST.
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