Careflow 7Fr x 20cm 3-lumen Central Venous Catheter Tray
FDA Recall Z-0630-05 · Posted 2005-03-18
Recalling FirmBecton Dickinson Infusion Therapy
Recall StatusTerminated
Product CodeFOZ
Date Initiated2005-01-10
Date Terminated2005-04-12
Product Quantity5 units
Reason for Recall
Various procedure trays and kits may have an insufficient seal, thus compromising sterility.
Firm Action
Customers were contacted by telephone and by letters dated 01/10/05.
Root Cause
Other
Distribution Pattern
Domestic distribution: WI. International distribution: Puerto Rico, Virgin Islands. There were no military or VA facilities.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.