Skip to content

NA 56-90614Recalls & reported problems

Stryker Leibinger GmbH & Co. KG · 1,5/1,7MM DYNAMIC MESH-STD-MEDIUM · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Mar 29, 2024Class IIOpen, Classified

    Mislabeled: Product labeled 56-90614 (90x90 Gold Mesh), was actually 56-90314 (90x90 Blue Mesh), may cause a delay in procedure

    Z-1785-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Plate, cranioplasty, preformed, alterable devices

All Plate, cranioplasty, preformed, alterable devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page