recall · 2026 incidents

13 documented incidents where type is recall and year is 2026, across 8 companies, 2026. Every row cites its source; severity runs S1 (near miss) to S5 (fatal or catastrophic). Entity pages: recall · 2026.

13Unique incidents

8Companies involved

S5Highest severity

85%Verified

38%From regulators

2026Years covered

Incident list

Sev	Date	Company	Type	Location	Incident	Source
S3	17 Jul 2026	Zoox	recall	Las Vegas, NV, USA	Zoox issues software recall after robotaxi drove into heavy smoke	CNBC
S3	17 Jul 2026	Zoox	recall	USA	Zoox recalls 105 robotaxis over heavy-smoke detection failure · 105 robotaxis recalled	Reuters
S3	20 Jun 2026	Zoox	recall	USA	Zoox Autonomous Vehicle Enters Smoke-Obscured Fire Scene, Prompting Recall · 105 vehicles recalled	Reuters
S3	18 Jun 2026	Waymo	recall	—	Waymo recalls 3,871 robotaxis over freeway construction-zone software defect · 3,871 vehicles	The Robot Report
S3	16 Jun 2026	WASP	recall	—	FDA Class II recall: Brand Name: WASPLab · Brand Name: WASPLab	openFDA enforcement
S2	09 Jun 2026	CMR Surgical	recall	—	Class II recall of Versius surgeon console over disabled Secure Boot cybersecurity control · 2 units distributed in the US (California)	FDA
S3	~Jun 2026	Waymo	recall	USA	Waymo recalls ~4,000 robotaxis after vehicles entered closed freeway construction zones	Austin American-Statesma
S3	~May 2026	Waymo	recall	USA	Waymo recalls robotaxi software over risk of driving into flooded roads	NBC 5 Dallas-Fort Worth
S3	20 Apr 2026	Waymo	recall	San Antonio, TX, USA	Unoccupied Waymo Robotaxi Swept Into Waterway After Entering Flooded San Antonio Road · 3,791 vehicles recalled	BBC News
S3	09 Apr 2026	WYBOT	recall	—	Robotic Pool Vacuum Fire Prompts CPSC Recall	Jersey Shore Online
S4	25 Mar 2026	Omnicell	recall	—	FDA Class I recall: Rolls of label stock used with the Omnicell i.v.Station. · Rolls of label stock used with the Omnicell i.v.Station.	openFDA enforcement
S5	11 Mar 2026	Intuitive Surgical	recall	—	Class I recall of da Vinci SureForm stapler reloads after patient death · 1 death, 4 serious injuries; recall of affected lot to customers who ordered on/before Feb 20, 2026	FDA
S3	21 Jan 2026	Auris Health (J&J MedTech)	recall	—	FDA Class II recall: MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-01 , MON-0 · MONARCH Platform, Bronchoscopy, Catalog Numbers: MON-000005-	openFDA enforcement

Companies involved

More recall views

More 2026 views

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