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Terminated

Zimmer brand Sirus Intramedullary femur nail system step reamer 0 mm, 6.5/4.5 mm cannulated, for cervical screws, item number 02.00020.039.

FDA Recall Z-0091-06 · Posted 2005-10-28

Recalling FirmZimmer Inc.
Recall StatusTerminated
Product CodeGFG
Date Initiated2005-09-30
Date Terminated2005-12-28
Product Quantity27

Reason for Recall

The calibrations on the reamers may lead to inaccurate reaming depth when used in accordance with the published surgical technique.

Firm Action

Consignees were notified via recall letter dated 9/30/05.

Root Cause

Other

Distribution Pattern

Arizona, California, Florida, Georgia, Illinois, Indiana, Kansas, Michigan, Minnesota, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Utah and Virginia.

Official Source

View FDA Recall →

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

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