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Terminated

Holt Probe Round Straight

FDA Recall Z-0540-06 · Posted 2006-02-23

Recalling FirmMedtronic Sofamor Danek Instrument Manufacturing
Recall StatusTerminated
Product CodeHXX
Date Initiated2005-12-22
Date Terminated2007-04-06
Product Quantity50 units

Reason for Recall

Depth indicators are incorrectly labeled (etched) on a measurement instrument.

Firm Action

The firm notified its direct consignees of the problem with the product and requested the return of any inventory via letter dated 12/22/05.

Root Cause

Other

Distribution Pattern

Nationwide, Japan, Hong Kong, Australia, The Netherlands Units - Domestic: 31, International: 19

Official Source

View FDA Recall →

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

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