RecallDepth

Ventra Percutaneous Intravenous Catheter Repair Kit for 11 French Triple-Lumen External Catheter Segment, Reorder Number 21-0107

Company
Deltec, Inc
Recall Initiated
July 8, 2003
Posted
July 30, 2003
Terminated
July 2, 2004
Recall Number
Z-1068-03
Firm Location
St Paul, MN

Reason for Recall

Silicone adhesive in kits used to repair damaged catheters did not set (cure) properly and remained in a tacky state.

Distribution

The product was shipped to 14 consignees (hospitals) in California, Illinois, Kansas, Michigan, Minnesota, Missouri, Pennsylvania, and Texas.

Lot / Code Info

Lot numbers M20691, 95311

Root Cause

Other

Action Taken

A recall letter, sent to the consignees on July 8, 2003, gave them the option of returning the kits or waiting for the firm to provide them with replacement silicone adhesive.

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