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Terminated

Careflow 14Ga x 20cm 2-lumen Central Venous Catheter Tray

FDA Recall Z-0629-05 · 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.

K033500BD CAREFLOW CENTRAL VENOUS CATHETERBecton, Dickinson & CO · 2004-01-29

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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