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Recall Observatory FDA recall evidence

Device product

Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S

Z-2407-2018

April 27, 2018

Class II

Product summary

Firm
Stryker GmbH
Event
Event 80131
Status
Terminated
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-2407-2018

Official wording

Reason: The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.

Code information: GTIN: 04546540673398; Lot code: K078C7E

Distribution pattern: The products were distributed to the following US states: AL, Co, FL, KY, NC, TN, UT, and WA.

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out-of-specification