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Medical Device

STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530

Recall date: 2026-08-12 · Source: FDA_DEVICE
Brand / Firm
Stryker Corporation
Product
STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
Reason for recall
There has been an increased amount in reported complaints consistently describing leaking from the handpiece during use.
Units affected
11,857 Units
Description
STRYKER PKG., SINGLE SPIKE TUBE SET, Catalog Number 0250070530
View official recall notice →