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

Consumer Product Safety Commission

Food and Drug Administration

National Highway Traffic Safety Administration

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

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

Olympus BiCOAG Hemostasis Probe 7Fr Coaxial Connector. Model Catalog Number: CD-B620LA

FDA30 Sept 2026

Brand match

Olympus Of The Americas

Markets

Tech & Electronics

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

Olympus BiCOAG Hemostasis Probe 7Fr Fixed Pin Connector. Model Catalog Number: CD-B622LA

FDA30 Sept 2026

Brand match

Olympus Of The Americas

Markets

Tech & Electronics

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

(Somofilcon A) Contact Lens

FDA30 Sept 2026

Brand match

Coopervision

Markets

Tech & Electronics

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234

FDA30 Sept 2026

Brand match

Philips Ultrasound

Markets

Tech & Electronics

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

Foresight elite tissue oximetry cable ref hemfsm10 UDI-di code: 00690103210927 the non-invasive foresight oximeter cable is intended for

FDA30 Sept 2026

Brand match

Becton Dickinson And

Markets

Tech & Electronics

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

Presource convenience kits: 1) kit, pre op , catalog number: amn548616a; 2) kit, nicu admit new han , catalog number: ba1dh0116b; 3) kit

FDA30 Sept 2026

Brand match

Cardinal Health 200

Markets

Tech & Electronics

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

Presource Convenience Kits: 1) KIT, USGPIV , Catalog Number: PVMHIVMHD; 2) KIT, USGPIV , Catalog Number: PVMHIVM14; 3) KIT, USGPIV

FDA30 Sept 2026

Brand match

Cardinal Health 200

Markets

Tech & Electronics

No image published for this recall

The official notice did not include a photo. Check the product details and identifiers below.

Medium

REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series

FDA30 Sept 2026

Brand match

Deroyal

Markets

Get alerted about these automatically

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.

Subscribe via RSS