Howmedica Osteonics Recalls

2 recalls found for Howmedica Osteonics. Check if any of your products are affected.

HIGHFDA DEVICE

Nov 12, 2025

Stryker Recalls CranialMask Tracker Due to Device Error

Stryker recalled 320 units of the CranialMask Tracker on November 12, 2025, due to software errors during surgery. The device fails to activate properly, displaying an error message that prevents its use. Healthcare providers must stop using this device and follow recall instructions immediately.

Howmedica Osteonics

When the

HIGHFDA DEVICE

Aug 28, 2025

Howmedica Osteonics Recalls Surgical Stems Due to Product Mix Risk

Howmedica Osteonics recalled 55 units of surgical stems on August 28, 2025, due to a potential product mix. Packages labeled as Catalog Number 0580-1-442 may contain Catalog Number 0580-1-352, leading to possible patient safety risks.

Howmedica Osteonics

a potential

Brand Statistics

Total Recalls

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