RecallRadar

FDA Device recall Z-2914-2018

AXS PP, 1X20MM BURR HOLE COVER, 2 X 2-HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01546S, for use on the cranium

On 2018-09-05 the FDA classified a Class II recall of AXS PP, 1X20MM BURR HOLE COVER, 2 X 2-HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01546S, for use on the cranium by Stryker Leibinger And Kg, citing after a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2914-2018
ClassificationClass II
Statusterminated
Initiated2018-06-22
Published2018-09-05
Last updated2026-09-13 11:54 UTC
CompanyStryker Leibinger And Kg
DistributionAZ, FL, NH, OH

Product

AXS PP, 1X20MM BURR HOLE COVER, 2 X 2-HOLE PLATES, 1.5X4mm SELF DRILLING SCREWS, Part Number 12-01546S, for use on the cranium

Reason

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

Identifiers

code_info1000201581, 1000215163, 1000230808, 1000252564, 1000256560, 1000259410, 1000260287, 1000263504, 1000211563, 1000267011, 1000267751

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2914-2018%22

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