RobotRisk Autonomous Systems Incident & Risk Register
RobotRisk / Stryker Mako / 2022-08-08
medical robotics · recall

Class II recall of Mako USB converter / Polaris Spectra camera tracking hardware

S2 · 08/08
2022 · Stryker Mako

Record

CompanyStryker Mako
Categorymedical robotics
Typerecall
Date08/08
2022
Time of daynot documented
Locationno physical site (recall / fleet-wide / aggregate record)
SeverityS2 (minor injury or single-unit damage)
ScaleMako tracking hardware components
Confidencemedium
VerificationCited source on file; not independently re-verified
SourceFDA

What happened

Stryker recalled the USB converter and Polaris Spectra camera used for optical tracking in the Mako Robotic-Arm Assisted Surgery System after identified device issues affecting tracking hardware reliability.

Stryker Mako record context

Entries by year and severity

14292018 S2: 11182020 S3: 1919202021 S3: 2929212022 S2: 12022 S3: 1213222023 S3: 1616232024 S3: 1515242025 S3: 2727252026 S3: 152026 S4: 11626
S1S2S3S4S5

By incident type

By severity

Stryker Mako vs medical robotics alternatives

medical robotics context

medical robotics: entries by year

2545082015 S2: 12015 S3: 12152016 S3: 32016 S4: 14162017 S4: 11172018 S2: 12018 S3: 12182019 S3: 33192020 S3: 1052020 S5: 3108202021 S3: 1642021 S4: 12021 S5: 3168212022 S2: 12022 S3: 1352022 S5: 10146222023 S3: 2222023 S5: 2224232024 S3: 2692024 S5: 7276242025 S3: 5042025 S5: 4508252026 S1: 12026 S2: 12026 S3: 4262026 S4: 52026 S5: 844126
S1S2S3S4S5

medical robotics: failure modes

medical robotics: most entries

recall context

recall: by category

recall: by year

recall: severity profile

Comparable recall events in medical robotics

SevDateCompanyEvent
S22026-06-09CMR SurgicalClass II recall of Versius surgeon console over disabled Secure Boot cybersecurity control
S42026-03-25OmnicellFDA Class I recall: Rolls of label stock used with the Omnicell i.v.Station.
S52026-03-11Intuitive SurgicalClass I recall of da Vinci SureForm stapler reloads after patient death
S32026-01-21Auris Health (J&J MedTech)FDA Class II recall: MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-0
S32025-09-12Noah MedicalFDA Class II recall: Brand Name: Galaxy System
S32025-05-23Quantum SurgicalFDA Class II recall: EPIONE Model 30-0001
S32025-04-23Virtual IncisionFDA Class II recall: MIRA SURGICAL SYSTEM, Table mounted miniaturized electromechanical sur
S32025-02-26Intuitive SurgicalClass II recall of da Vinci 5 foot pedal over spring failure

Other Stryker Mako entries

Also from Critical Systems Analysis: CSA - functional safety engineering · Company directory · FSTalent - functional safety jobs