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Recall Observatory FDA recall evidence

Device product

INSTRUMENT TRACKER 9733533XOM ENT 1PK

Z-1586-2014

April 24, 2014

Class II

Product summary

Firm
Medtronic Navigation, Inc.
Event
Event 68145
Status
Terminated
Classification
Class II
Quantity
26,674 total
Official record key
device-enforcement:Z-1586-2014

Official wording

Reason: Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.

Code information: Lot No.: 130904C 131203A 131003 131024B 130815 130904C 130510 130815 130708B 130815 130815 130716D 130204C 130418B 121128C 121218B 121218A 121128D 130409C 130409D 130123

Distribution pattern: Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Medtronic Navigation is recalling certain Medtronic single-use, disposable devices because there was not sufficient control to assure that returned, unused devices were appropriately examined for product and/or package damage to ensure sterility.