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

Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS)

FDA23 Sept 2026

Brand match

Maquet Cardiopulmonary

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

Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS)

FDA23 Sept 2026

Brand match

Maquet Cardiopulmonary

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

Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS)

FDA23 Sept 2026

Brand match

Maquet Cardiopulmonary

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

MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT

FDA23 Sept 2026

Brand match

Bayer Medical Care

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

NOxBOXi Nitric Oxide Delivery System

FDA23 Sept 2026

Brand match

Noxbox

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

Centricity Enterprise Archive V2, V3, and V4, software product for receiving, archiving, and sending electronic medical data, All Versions

FDA23 Sept 2026

Brand match

GE Healthcare

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

Enterprise Archive V8, software product for receiving, archiving, and sending electronic medical data, All versions

FDA23 Sept 2026

Brand match

GE Healthcare

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

Centricity PACS V2, V3, V4, V6, V7, software product is intended for the storage, reading, diagnostic review, analysis, annotation

FDA23 Sept 2026

Brand match

GE Healthcare

Markets

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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.

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