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Recall2026-08-26China DPRCsamrdprc:20260827_115936aigo-brand H872SPW and H875SPW "H8" drones
aigo-brand H872SPW and H875SPW "H8" drones — 15 units built between 26 May and 22 Jul 2025 recalled because geofencing, sense-and-avoid and electromagnetic compatibility all fail GB 42590-2023, China's civil UAS safety standard. Filed with the Jiangxi provincial market regulator. The regulator's stated risk is that the aircraft can enter restricted airspace and is more prone to mid-air collision. Free repair, part replacement or return.
cause not establishedsamrdprc:20260827_115936Read the record ↗Recall2026-06-22Health CanadaRA-82239CyberKnife Treatment Delivery System
CyberKnife Treatment Delivery System — Type II recall: performance malfunction can occur when the collimator housing is moved over the Xchange table, causing the robot to lock up and halt operation. Affects 4 system units (lots C0417, C0545, C0573, C0351). Facilities told to clear the treatment area, not move the robot via the in-room pendant, and contact Accuray service. No injuries reported.
cause not establishedRA-82239Read the record ↗Recall2026-04-09CPSCWYBOT26372Wybotics Recalls Robotic Pool Vacuums Due to Burn and Fire Hazards
Wybotics Recalls Robotic Pool Vacuums Due to Burn and Fire Hazards — Hazard: The lithium-ion battery in the recalled pool vacuums can overheat, posing burn and fire hazards to consumers. Reported incidents: The firm has received ten reports of the pool vacuums overheating or catching fire while charging and not charging, resulting in nine incidents of property damage. No injuries have been reported.
cause attributed by source26372WYBOTRead the record ↗Recall2026-02-19Health CanadaRA-81627Monarch Platform (Model MON-000006)
Monarch Platform (Model MON-000006) — Type II recall: rare software glitch where the app may restart during procedure setup, resetting patient-side state to patient-left if it had been set to patient-right, risking unintended robotic-arm movement toward the wrong anatomical side. No injuries reported; facilities told to contact the manufacturer.
cause not establishedRA-81627Read the record ↗Recall2026-02-19Health CanadaRA-81626Hugo RAS Bipolar Maryland Forceps and Hugo RAS Bipolar Fenestrated Grasper
Hugo RAS Bipolar Maryland Forceps and Hugo RAS Bipolar Fenestrated Grasper — Voluntary safety notice: increased likelihood of drive-cable pulley-assembly component failure due to manufacturing variations, which can make instrument jaw control incorrect/uncontrolled and may detach a white plastic pulley component inside the patient's body. The Hugo RAS system automatically detects and halts control of the affected instrument when this occurs. No injuries reported.
cause not establishedRA-81626Read the record ↗