Home / Recalls / Stryker Instruments Div. of Stryker Corporation / Z-1244-2018

Z-1244-2018 Class II Terminated

Recalled by Stryker Instruments Div. of Stryker Corporation — Portage, MI

Recall Details

Product Type
Devices
Report Date
April 4, 2018
Initiation Date
November 9, 2017
Termination Date
April 16, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
708

Product Description

180-Gram Cement Cartridge with Breakaway Femoral Nozzle, Product Number: 0206-530-000, UDI: (01)4546540857880 for orthopedic use.

Reason for Recall

Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates.

Distribution Pattern

Distributed in all 50 U.S. States and the District of Columbia. Distributed in Australia, Argentina, Japan, Canada, Chile, Korea, Spain, France, Italy, Netherlands, and United Kingdom.

Code Information

Lot Numbers: 17277012, 17283012 UDI: (01)4546540857880

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