Stryker Corporation: Medical Device Recall in 2025 - (Recall #: Z-0982-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 28, 2023

Date Posted: January 29, 2025

Recall Number: Z-0982-2025

Event ID: 95998

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).

Status: Ongoing

Product Quantity: 1489 units

Code Information:

GTIN 07613154028177, Lot Numbers: 22179047, 22179027, 22160017

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated