Stryker Leibinger GmbH & Co. KG recalls
Every recall we track for Stryker Leibinger GmbH & Co. KG — 23 in all, from 2018–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Stryker Leibinger GmbH & Co. KG peaked in 2018 (18); 23 since 2017.
All FDA recall records for Stryker Leibinger GmbH & Co. KG since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 18 | 0 | 18 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 2 | 0 | 2 |
| 2022 | 0 | 0 | 0 | 1 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 2 | 0 | 2 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Stryker Leibinger GmbH & Co. KG product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Stryker Leibinger GmbH & Co. KG recalls
6 shown- Lower riskMedical device
Stryker Leibinger GmbH & Co. KG recalls 8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a next-generation
Stryker recalls ENT software version NOVA 3.6.0 RC16 for visual feedback errors during sinus surgery. Affected units may show incorrect points relative to physical reference points.
StrykerApr 4, 2024 - Lower riskMedical device
Stryker Leibinger GmbH & Co. KG recalls Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the
Stryker recalls 1.5/1.7MM Dynamic Mesh (56-90614) due to mislabeling as 90x90 Gold Mesh when it's actually 90x90 Blue Mesh, potentially delaying surgical procedures.
StrykerMar 29, 2024 - UnratedMedical device
Stryker Leibinger GmbH & Co. KG recalls Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis
Stryker recalls unapproved TMJ reconstruction prosthesis models. This device was shipped without regulatory approval, posing potential safety risks.
StrykerDec 6, 2022 - Lower riskMedical device
Stryker Leibinger GmbH & Co. KG recalls MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032
Stryker recalls MEDPOR Titan OFW - MTB Right 1.0mm implants with a packaging error where the barrier layer is on the wrong side. This could affect surgical placement. Check your implant's UDI and lot number.
StrykerDec 29, 2021 - Lower riskMedical device
Stryker Leibinger GmbH & Co. KG recalls DirectInject consists of a sterile dual paste system which is calcium phosphate based. Upon injection through the
Stryker Leibinger recalls DirectInject cement paste system due to inability to inject paste into target location. Affected units have specific lot numbers and product codes.
Stryker Leib:ingApr 1, 2021 - Lower riskMedical device
Stryker Leibinger GmbH & Co. KG recalls AXS PP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01540S, for use on the cranium
Stryker recalls AXS PP cranium plates with potential packaging compromise after three years. Affected units include specific part numbers; contact for return instructions.
StrykerJun 22, 2018
Stryker Leibinger GmbH & Co. KG recall questions
How many recalls has Stryker Leibinger GmbH & Co. KG had?
23 recalls from Stryker Leibinger GmbH & Co. KG are on record with U.S. safety agencies, from 2018–2024.
What is the most recent Stryker Leibinger GmbH & Co. KG recall?
Stryker Leibinger GmbH & Co. KG recalls 8000-021-002, Scopis¿ ENT Software with TGS¿ with Sofware Version: NOVA 3.6.0 RC16. Scopis is a next-generation, dated Apr 4, 2024. Every Stryker Leibinger GmbH & Co. KG recall is listed on this page, newest first.
What should I do if I have a recalled Stryker Leibinger GmbH & Co. KG product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Stryker Leibinger GmbH & Co. KG recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.