Surgical Theater recalls

Surgical Theater has 7 recalls on record with the FDA and USDA, the earliest in 2025 and the latest reported on 5 Nov 2025. 7 were reported in the last 12 months. The most frequent reason is lead & heavy metals.

Total recalls7since 2025

Last 12 months7reported

Class I00% of total

Ongoing0latest 5 Nov 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 7 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 7 100%Class III 0 0%

Why surgical theater is recalled

Lead & Heavy Metals7100%

Product types

Surgical Instruments571%
Hip & Knee Implants229%

By year

20257100%

All surgical theater recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
5 Nov 2025Device	CLASS II	SyncAR Surgical Navigation Advanced Platform Patient recalled	Surgical Theater	Lead & Heavy Metals	Nationwide
5 Nov 2025Device	CLASS II	Surgical Navigation Advanced Platform Patient Engagement (PE SNAP) recalled	Surgical Theater	Lead & Heavy Metals	Nationwide
5 Nov 2025Device	CLASS II	Surgical Navigation Advanced Platform (SNAP) recalled	Surgical Theater	Lead & Heavy Metals	Nationwide
5 Nov 2025Device	CLASS II	SpineAR Surgical Navigation Advanced Platform Patient recalled	Surgical Theater	Lead & Heavy Metals	Nationwide
5 Nov 2025Device	CLASS II	Endo Surgical Navigation Advanced Platform Patient recalled	Surgical Theater	Lead & Heavy Metals	Nationwide
5 Nov 2025Device	CLASS II	Surgical Planner, BrainSTORM recalled by Surgical Theater	Surgical Theater	Lead & Heavy Metals	Nationwide
5 Nov 2025Device	CLASS II	SuRgical Planner (SRP) recalled by Surgical Theater	Surgical Theater	Lead & Heavy Metals	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.