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Terminated

BD First PICC 3F 65 cm Single Lumen Procedure Kit.

FDA Recall Z-0832-03 · Posted 2003-05-15

Recalling FirmBecton Dickinson Infusion Therapy
Recall StatusTerminated
Product CodeLJS
Date Initiated2003-04-04
Date Terminated2003-07-30
Product Quantity840 kits

Reason for Recall

A 4 Fr catheter was packaged in PICC convenience kits labeled as 3 Fr.

Firm Action

All distributors and known hospitals were notified on 04/04/2003 by telephone, followed by a fax notification.

Root Cause

Other

Distribution Pattern

Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K945499CATO FIRST PICC KITCatco Medical, Inc. · 1995-02-07

Official Source

View FDA Recall →

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

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