FDA recall record

Stryker T2 Tibia System Nail Insertion Sleeve, Elastic, Sterile, a) REF 1806-1406S, SPI recall — FDA Z-0065-2015

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

Class IIclassification
Z-0065-2015official record ID
Oct 22, 2014report date

Recall record at a glance

Official recordZ-0065-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmStryker Howmedica Osteonics Corp.
Report dateOct 22, 2014
Recall initiation dateJul 24, 2014
Quantity484 units
LocationMahwah, NJ, United States

Official product description

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.

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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