Stryker Leibinger GmbH & Co. KG: Medical Device Recall in 2018 - (Recall #: Z-2904-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01530S, for use on the cranium

Product Classification:

Class II

Date Initiated: June 22, 2018

Date Posted: September 5, 2018

Recall Number: Z-2904-2018

Event ID: 80371

Reason for Recall:

After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.

Status: Terminated

Product Quantity: 22,831 total

Code Information:

1000107793, 1000107794, 1000107795, 1000111407, 1000113293, 1000119681, 1000119682, 1000124116, 1000130031, 1000134145, 1000139203, 1000141585, 1000148808, 1000150571, 1000156031, 1000159892, 1000166365, 1000168534, 1000169198, 1000170705, 1000171359, 1000174838, 1000176391, 1000183609, 1000188544, 1000189237, 1000191063, 1000193586, 1000195789, 1000202429, 1000215159, 1000217674, 1000220165, 1000224225, 1000231906, 1000233773, 1000236827, 1000239654, 1000245176, 1000251377, 1000254803, 1000262514

Distribution Pattern:

US distribution in the states: AZ, FL, NH, and OH, Australia, Canada, France, New Zealand, and UK.

Voluntary or Mandated:

Voluntary: Firm initiated