Class II

Medical Device Recall: stryker 3.0MM Precision Neuro Match Head, REF 5820-107-530, used to cut bone and bone cement during neurosurgery

Stryker Corporation · June 28, 2023

Reason for Recall

There is potential the device inside the package may not match the product information on the outer label (e.g., label states 5820-107-430 but package contains a 5820-107-530 device or vice versa).

Distribution

Worldwide distribution - US Nationwide and the countries of UK, Netherlands, New Zealand.

States Affected

NATIONWIDE

Quantity Affected

1489 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0982-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.