United States Tech & Electronics recalls

Latest official safety notices for United States.

What this United States tech & electronics recalls feed covers

This page lists tech & electronics recalls and safety alerts from official sources relevant to United States. Each notice links back to the original official source.

Start with a recall below to review the affected products, identifiers and dates, then follow the action described in the official notice.

RecallScope is not affiliated with any government agency or regulator — we list what official public sources publish, so always check the original notice before acting on an alert.

Where these recalls come from

Updated from official United States public sources. Always open the original notice for the full product list.

Latest United States Tech & Electronics recalls

Most recent safety alerts, newest first.

Tech & Electronics
Medium

Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250; Intellijoint HIP

FDA14 Oct 2026

Brand match

Intellijoint Surgical

Markets

US
Tech & Electronics
Low

EPM Series Patient Monitor. Patient Monitor Series: ePM 10M ePM 12M ePM 12MA ePM 15M ePM 10A

FDA14 Oct 2026

Brand match

Mindray Ds

Markets

US
Tech & Electronics
Low

BeneVision N1 and N-Series Patient Monitor. Patient Monitor: N12 N15 N17 N19 N22

FDA14 Oct 2026

Brand match

Mindray Ds

Markets

US
Tech & Electronics
Low

BeneVision Series Telemetry Monitor. Operators Manuals: TM70 TM80

FDA14 Oct 2026

Brand match

Mindray Ds

Markets

US
Tech & Electronics
Low

Panorama and Telemetry Monitoring System. Operators Manuals: TMS-6016 Panorama Telepack-608 TMS60 (TD60)

FDA14 Oct 2026

Brand match

Mindray Ds

Markets

US
Tech & Electronics
Low

BeneView Series. Operators Manuals: T5 T8

FDA14 Oct 2026

Brand match

Mindray Ds

Markets

US
Tech & Electronics
Low

Passport Series Patient Monitor. Operators Manuals: 8 12 12M 17M V

FDA14 Oct 2026

Brand match

Mindray Ds

Markets

US
Tech & Electronics
Low

CPM Series Patient Monitor. Operators Manual: cPM 8 cPM 12

FDA14 Oct 2026

Brand match

Mindray Ds

Markets

US

Frequently asked questions

A recall is an official notice that a product may create a safety risk or does not meet a required standard. The notice explains which products are affected and what action to take.
Open the recall and compare its product name, model, batch, serial number, VIN or other identifiers with the item you own.
Follow the action in the official notice. Depending on the recall, this may mean stopping use, returning the product, contacting the supplier or booking a repair.