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Recall Observatory FDA recall evidence

Device product

Total Knee Arthroplasty (TKA) 2, Total Knee Arthroplasty (TKA) 1, Partial Knee Arthroplasty (PKA) 3, Total Hip Arthroplasty (THA) 4.0, 4.1 on Mako 3.0, 3.1. Software: TKA 2.0 + TKA 1.0.1 + THA 4.1 + PKA 3.0.2 + MGO 1.2.2 Application Part Number: 700001590414

Z-1911-2024

April 15, 2024

Class II

Product summary

Firm
Stryker Orthopaedics
Event
Event 94473
Status
Ongoing
Classification
Class II
Quantity
1,635 units
Official record key
device-enforcement:Z-1911-2024

Official wording

Reason: Application software intended to be deployed on Mako 3.0, part number 209999, and Mako 3.1, part number 219999, observed an increase in the Software Error #3 (SE3) error code when a Mako System shutdown or a Mako System restart is not performed prior to switching between applications (i.e. TKA to THA), resulting in delay in treatment

Code information: UDI-DI: (01)7613327566444(10). Software: TKA 2.0 + TKA 1.0.1 + THA 4.1 + PKA 3.0.2 + MGO 1.2.2. Application Part Number: 700001590414. Revision: AA, AB, & AC.

Distribution pattern: Worldwide - US Nationwide and the countries of Australia, Austria, Belgium, Canada, Chile, China, Columbia, Denmark, Finland, France, Germany, Greece, India, Israel, Italy, Japan, Korea, Kuwait, Luxembourg, Malaysia, Mexico, Netherlands, New Zealand, Puerto Rico, Qatar, Romania, Saudi Arabia, Singapore, Spain, South Africa, Sweden, Switzerland, Thailand, Turkey, UAE, and UK

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Software Error #3 (SE3) error