Howmedica Osteonics Recalls

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

Health & Personal Care
HIGH
FDA DEVICE

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
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Health & Personal Care
HIGH
FDA DEVICE

Howmedica Osteonics Recalls 55 EXETER V40 Surgical Stems Due to Product Mix Risk

Howmedica Osteonics recalled 55 units of EXETER V40 surgical stems distributed in the United Kingdom due to a risk of product mix. Patients may receive the incorrect product, potentially leading to surgical complications. Patients and healthcare providers must stop using the device and follow the manufacturer’s instructions.

Howmedica Osteonics
a potential
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Brand Statistics

Total Recalls
2
Pages
1

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