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FDA Medical Device Recalls (openFDA)

Stryker Leibinger GmbH & Co. KG: AXS PP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01541S, for use on the cranium

Recall number
Z-2911-2018
Recalling firm
Stryker Leibinger GmbH & Co. KG
Product
AXS PP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF TAPPING SCREWS, Part Number 12-01541S, for use on the cranium
Status
Terminated
Initiated
2018-06-22
Posted
not on file
Terminated
2019-07-08
Reason
After a three year term, there is a potential for the external packaging (sterile barrier) to become compromised.
Root cause
Package design/selection
Action
URGENT MEDICAL DEVICE RECALL letters dated 6/22/18 were sent to customers with the following requested actions to be taken: 1. Please inform users of this Medical Device Removal and pass this notice to all appropriate individuals within your organization. 2. Return all affected products available at your location to: Stryker CMF Attn: Recall Coordinator 6300 Sprinkle Rd Portage, MI 49002 REF: PFA #1739180 Or, Contact Stryker Customer Service and refer to PFA #1739180 with any questions about returning the product to us. 3. Complete and sign the enclosed Business Reply Form and fax a copy to: (877) 648-7114 or email a copy to CMF-custserv@stryker.com. 4. Keep a copy of the completed and executed Customer response Form for your records.
Quantity
22,831 total
Distribution
US distribution in the states: AZ, FL, NH, and OH, Australia, Canada, France, New Zealand, and UK.
Lot, serial or model codes
1000201582, 1000254804, 1000258650, 1000259408, 1000261022, 1000262518, 1000262519
510(k) numbers
["K120352"]
PMA numbers
not on file
Product code
GWO
Firm FEI
3002821504
Firm city
Freiburg Im Breisgau
Firm state
not on file
Firm country
Germany

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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