Skip to content

NA 2296003155Recalls & reported problems

Stryker Corporation · Precision Thin (9.0 x 0.38 x 18.5mm) · Class 1

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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Jan 8, 2025Open, Classified

    Precision Thin blade attachments have a potential to be out of measurement specifications, preventing them from securely fitting into the compatible handpiece.

    Z-1139-2025 · Root cause: Process control · FDA record ↗

Other BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL devices

All BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.