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Terminated

Introcan Safety IV Catheter 22G x 1'' PUR with Wings. The affected catalogs and lot numbers: Catalog Number 4253540 - Lot number 3G26258U02 Catalog Number 4253540 - Lot number 3G27258U02

FDA Recall Z-1092-04 · Posted 2004-07-20

Recalling FirmBraun,B Medical Inc
Recall StatusTerminated
Product CodeFOZ
Date Initiated2004-03-19
Date Terminated2004-09-21
Product Quantity86 units

Reason for Recall

Mislabeled product. The recalling firm received a complaint that a box of Introcan Safety Catheters, (22G x 1 inch) contained mixed 18G catheters with the same lot number.

Firm Action

The recalling firm received a product complaint of a mixed 18G Catheters with 22G Catheters.

Root Cause

Other

Distribution Pattern

The affected recalling units were distributed nationwide to the following states: AZ, CA, GA, IL, IN, MD, OH, OK, OR, MA, MI, NC, NJ, NY, OR, PA, TX, UT, VA, WI

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K020785INTROCAN SAFETY IV CATHETERB.Braun Medical, Inc. · 2002-08-28K982805INTROCAN SAFETY IV CATHETERB.Braun Medical, Inc. · 1999-01-14

Official Source

View FDA Recall →

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

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