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Terminated

Trident Insert Impactor

FDA Recall Z-0901-03 · Posted 2003-05-29

Recalling FirmStryker Howmedica Osteonics
Recall StatusTerminated
Product CodeHWA
Date Initiated2003-04-28
Date Terminated2003-11-12
Product Quantity1758

Reason for Recall

The ball retaining sleeve on the Trident Insert Impactor can possibly disassemble.

Firm Action

Howmedica sent recall letters and acknowledgement forms via FedEx on April 29, 2003 with return receipt.

Root Cause

Other

Distribution Pattern

The product has been distributed the Howmedica branches and sales reps, hospitals, and International Howmedica distributors located in Sweden, China, France, Netherlands, Germany, Spain, Australia, Japan, New Zealand, Switzerland, Portugal, England, Chile, and Brazil.

Official Source

View FDA Recall →

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

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