Class II — Potential Health Hazard

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

Veradius Unity Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to Firm discovered that the wireless foot switch can...

Date: December 2, 2021
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

Veradius Unity, Model #718132

Quantity: 12 US; 44 ROW

Why Was This Recalled?

Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if the hand switch is not used or if the wired foot switch is not connected to the system.

Where Was This Sold?

This product was distributed to 26 states: AZ, CA, FL, GA, HI, IL, KS, KY, ME, MD, MA, MI, MN, MS, NE, NV, NJ, NY, NC, OH, PA, TN, TX, VA, WA, WV

Affected (26 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