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Terminated

BD L-Cath EX (20ga x 15cm), L-Cath Catheter System

FDA Recall Z-0784-04 · Posted 2004-07-20

Recalling FirmBecton Dickinson Infusion Therapy
Recall StatusTerminated
Product CodeLJS
Date Initiated2004-03-09
Date Terminated2011-06-24
Product Quantity580 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.

K920755L-CATH PEEL AWAY SYSTEM CATHETERLuther Medical Products, Inc. · 1993-06-07

Official Source

View FDA Recall →

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

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