Lower riskMedical device recall · FDA · Published March 29, 2024
Stry: 1.5/1.7MM Dynamic Mesh Recall - Mislabeled Product May Delay Surgery
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.
Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure
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📍Recalling firmStryker Leibinger GmbH & Co. KGBotzinger Str. 41 · Freiburg Im Breisgau, Germany
✎ GovInfoNow plain-language explainer
Stryker is recalling a specific type of surgical mesh product because it was mislabeled. This could cause delays in surgical procedures if the wrong mesh is used. The recall affects products sold with the catalog number 56-90614. Read more at govinfonow.com/recall/55681-stry-1-5-1-7mm-dynamic-mesh-recall-mislabeled-product.
“Stry: 1.5/1.7MM Dynamic Mesh Recall - Mislabeled Product May Delay Surgery.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55681-stry-1-5-1-7mm-dynamic-mesh-recall-mislabeled-product. Based on FDA recall #Z-1785-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1785-2024%22&limit=1).
The FDA announced on March 29, 2024, that Stryker Leibinger GmbH & Co. KG is recalling Stryker 1,5/1,7MM DYNAMIC MESH products due to mislabeling that may delay surgical procedures. The agency issued recall number Z-1785-2024 for the Class II device distributed nationwide.
The product labeled as 56-90614 (90x90 Gold Mesh) was actually 56-90314 (90x90 Blue Mesh). This mislabeling may cause a delay in procedure, according to the FDA.
Context
GovInfoNow's records show Stryker Leibinger GmbH & Co. KG has 5 other recalls on record since June 22, 2018. Other recent recalls of similar products include Stryker Scopis ENT Software Version NOVA 3.6.0 RC16 (April 4, 2024), Stryker TMJ Reconstruction Prosthesis (December 6, 2022), and Stryker MEDPOR Titan OFW - MTB Right 1.0mm (December 29, 2021). Additional recent recalls of similar products include Tornier Perip Screw (December 19, 2025), W L Gore GORE VIABIL Short Wire Biliary Endoprosthesis (May 22, 2026), and Stryker FluidSmart Urology Tube Set (April 9, 2026).
How to tell if you have this one
Check for the catalog number 56-90614 on the product packaging. The product is intended for cranial bone reconstruction and stabilization.
Brand
Stryker
Product
Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the catalog number 56-90614 on the product packaging to confirm it's the recalled item.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 47 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1785-2024 (March 29, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1785-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.