Class II — Potential Health Hazard

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

Velara Generator with an old Firmware version used with the Recalled by Philips Electronics North America Corporation Due to System may lock up.

Date: December 9, 2016
Company: Philips Electronics North America Corporation
Status: Terminated
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 Electronics North America Corporation directly.

Affected Products

Velara Generator with an old Firmware version used with the Philips Integris BH5000

Quantity: 59 devices (this number represents all products listed in recall)

Why Was This Recalled?

System may lock up.

Where Was This Sold?

This product was distributed to 16 states: AL, CA, GA, IL, KS, MD, MO, NY, NC, OH, PA, RI, SC, TX, WA, DC

Affected (16 states)Not affected

About Philips Electronics North America Corporation

Philips Electronics North America Corporation has 160 total recalls tracked by RecallDetector.

Related Recalls

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