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Terminated

TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016.

FDA Recall Z-0659-03 · Posted 2003-03-20

Recalling FirmInterpore Cross International Inc
Recall StatusTerminated
Product CodeLXH
Date Initiated2003-02-07
Date Terminated2003-08-28
Product Quantity37 units

Reason for Recall

Instrument fell apart during cleaning prior to surgery.

Firm Action

Firm telephoned customers on 2/7/2003 requesting that they immediately return thier instruments.

Root Cause

Other

Distribution Pattern

States of NJ, CA, PA, MN, WI, MO, FL, OH, VA, MD, Wash DC, NY, CO, MA and to Brazil, Mexico, England, Denmark, Belgium, Australia.

Official Source

View FDA Recall →

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

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