Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Philips Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Potential for the Mains Control Unit board fuse...

Date: October 7, 2024
Company: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. directly.

Affected Products

Philips Zenition 70, Model Number: 718133

Quantity: 2,247 units (582 US, 84 Canada, 1,581 R.O.W.)

Why Was This Recalled?

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has 154 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report