Class II — Potential Health Hazard

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

BrightView product code: 882478 BrightView X product code: 882480 BrightView Recalled by Philips Medical Systems (Cleveland) Inc Due to Software issues

Date: November 4, 2014
Company: Philips Medical Systems (Cleveland) Inc
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 Medical Systems (Cleveland) Inc directly.

Affected Products

BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454

Quantity: 85

Why Was This Recalled?

Software issues

Where Was This Sold?

This product was distributed to 17 states: AR, CA, FL, GA, ID, LA, ME, MI, MN, MS, MO, NJ, NY, OH, OK, PA, TX

Affected (17 states)Not affected

About Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc has 313 total recalls tracked by RecallDetector.

Related Recalls

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