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Recall Observatory FDA recall evidence

Device product

Stryker, T2 K-Wire, 3.2x400mm, CoCr, Recon Product Usage: Intended for the temporary stabilization of bone segments or fragments.

Z-0884-2016

January 21, 2016

Class II

Product summary

Firm
Stryker Howmedica Osteonics Corp.
Event
Event 73156
Status
Terminated
Classification
Class II
Quantity
147,838 units in total
Official record key
device-enforcement:Z-0884-2016

Official wording

Reason: During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.

Code information: Catalog number 1806-3031S; All lots distributed before 10 Nov 2015 with non-expired 5 year shelf life

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.