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recall · 2024 incidents

11 documented incidents where type is recall and year is 2024, across 9 companies, 2024. Every row cites its source; severity runs S1 (near miss) to S5 (fatal or catastrophic). Entity pages: recall · 2024.

11Unique incidents
9Companies involved
S3Highest severity
55%Verified
55%From regulators
2024Years covered

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Incident list

SevDateCompanyTypeLocationIncidentSource
S319 Dec 2024Intuitive Surgical recall —Class II recall of da Vinci reusable instruments (forceps, scissors, drivers, graspers) over cable fraying · multiple instrument models, US and international distribution MedTech Dive
S328 Oct 2024Noah Medical recall —FDA Class II recall: Galaxy System (GAL-001). · Galaxy System (GAL-001). openFDA enforcement
S119 Aug 2024Kinova Robotics recall —Kinova Jaco assistive robotic arm - FDA Class I correction for fire/burn hazard · All lots/serial numbers of affected Jaco arm models FDA Medical Device Recal
S309 Aug 2024Cruise recall USAGM's Cruise recalls entire robotaxi fleet over unexpected braking Wards Auto
S305 Aug 2024Quantum Surgical recall —FDA Class II recall: The EPIONE device v1.0.2 is a user controlled, stereotactic accessory · The EPIONE device v1.0.2 is a user controlled, stereotactic openFDA enforcement
S302 Aug 2024Auris Health (J&J MedTech) recall —FDA Class II recall: Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. · Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005 openFDA enforcement
S321 May 2024Waymo recall Phoenix, AZ, USAWaymo recalls robotaxis after collision with utility pole · fleet-wide software update TechCrunch
S315 Apr 2024Stryker Mako recall —Class II recall of Mako 3.0/3.1 software over error #3 causing loss of robotic function mid-surgery · Mako 3.0 and 3.1 software, field correction to installed base MassDevice
S309 Mar 2024Noah Medical recall —FDA Class II recall: Galaxy System REF GAL-001 (specifically GAL-019, Wired Controller) · Galaxy System REF GAL-001 (specifically GAL-019, Wired Contr openFDA enforcement
S314 Feb 2024Globus Medical recall —FDA Class II recall: ExcelsiusGPS Cannula A, 9mm x 250mm, Cannula used with ball tip probes · ExcelsiusGPS Cannula A, 9mm x 250mm, Cannula used with ball openFDA enforcement
S3~Feb 2024Waymo recall —Waymo recalls 444 vehicles over towed-vehicle detection issue · 444 vehicles NBC News

Companies involved

Noah Medical 2Waymo 2Intuitive Surgical 1Kinova Robotics 1Cruise 1Quantum Surgical 1Auris Health (J&J MedTech) 1Stryker Mako 1Globus Medical 1

More recall views

S3 and above (69)Medical robotics (36)AV trucking (19)2025 (14)2026 (13)

More 2024 views

2024 (77)S3 and above (50)AV trucking (29)S4 and above (28)Other (16)crash (14)S5 fatal or catastrophic (12)fatality (11)malfunction (11)
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