Z-0873-2016 Class II Terminated

Recalled by Stryker Howmedica Osteonics Corp. — Mahwah, NJ

Recall Details

Product Type
Devices
Report Date
March 2, 2016
Initiation Date
January 21, 2016
Termination Date
June 8, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
147,838 units in total

Product Description

Stryker, T2 K-Wire, 3x285 mm Product Usage: Intended for the temporary stabilization of bone segments or fragments.

Reason for Recall

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

Distribution Pattern

US Nationwide Distribution

Code Information

Catalog number 1806-0050S; All lots distributed before 10 Nov 2015 with non-expired 5 year shelf life