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Recall Observatory FDA recall evidence

Device product

Stryker T2 Tibia System Nail Insertion Sleeve, Elastic, Sterile, a) REF 1806-1406S, SPI 08-11 and b) REF 1806-1407S, SPI 08-13. Product Usage: The T2 Tibial Nailing system is intended to provide temporary stabilization of various types of fractures, malunion and nonunion of the tibia. The nails are inserted using an opened or closed technique and can be statically, dynamically and compressed locked. The system is indicated for long bone fracture fixation, specifically tibial fracture fixation. The sleeves are intended to ease nail insertion and to protect the condyle surfaces during nail insertion.

Z-0065-2015

July 24, 2014

Class II

Product summary

Firm
Stryker Howmedica Osteonics Corp.
Event
Event 69065
Status
Terminated
Classification
Class II
Quantity
484 units
Official record key
device-enforcement:Z-0065-2015

Official wording

Reason: Stryker Orthopaedics received a report indicating some of the Nail Insertion Sleeves had a different inner diameter than described on the package label.

Code information: Catalog #1806-1406S - Lot #'s K019A3C, K031467, K032811, K032812, K06AAA8, K07F95F and K083672, expiry date 3/31/2019 and Catalog #1806-1407S - Lot #'s K031468, K03E8AD and K074529, expiry date 3/31/2019

Distribution pattern: US Nationwide Distribution in the states of CA, FL, IN, MD, NC, NH, NY, OH, PA and WI.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Stryker Orthopaedics received a report indicating some of the Nail Insertion Sleeves had a different inner diameter than described on the package label.