BD L-Cath EX (28ga x 20cm), L-Cath Catheter System
FDA Recall Z-0785-04 · Posted 2004-07-20
Recalling FirmBecton Dickinson Infusion Therapy
Recall StatusTerminated
Product CodeLJS
Date Initiated2004-03-09
Date Terminated2011-06-24
Product Quantity1850 units
Reason for Recall
Catheters have stylets extending past the catheter tip, which, if not noticed could cause injury upon insertion.
Firm Action
All consignees were notified by telephone on 03/09/2004, followed by a fax letter.
Root Cause
Other
Distribution Pattern
Nationwide. Foreign distribution to Australia, Canada and Japan.
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.