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Terminated

Atlantis Anterior Cervical Plate System Screw Driver, Part number 876-482

FDA Recall Z-0330-06 · Posted 2005-12-28

Recalling FirmMedtronic Sofamor Danek Instrument Manufacturing
Recall StatusTerminated
Product CodeHXX
Date Initiated2005-11-28
Date Terminated2006-11-09
Product Quantity75 units

Reason for Recall

Screwdriver handle breakage

Firm Action

The recalling firm sent out a letter dated 12/01/2005 explaining the problem and requesting return of the product.

Root Cause

Other

Distribution Pattern

IL, IN, MI, CA, Japan, Netherlands

Official Source

View FDA Recall →

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

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