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 DigitalDiagnost software 4.1.x and 4.2.x Recalled by Philips Medical Systems Gmbh, DMC Due to Stitching run on SkyPlate detector interrupted intermittently; Stitching...

Date: September 19, 2018
Company: Philips Medical Systems Gmbh, DMC
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 Gmbh, DMC directly.

Affected Products

Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712032701032, 712033, 712224, 712225, 712226, 712227, 712228.

Quantity: 829 units

Why Was This Recalled?

Stitching run on SkyPlate detector interrupted intermittently; Stitching with SkyPlate aborts after first image; System software CD contains wrong baseline

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Philips Medical Systems Gmbh, DMC

Philips Medical Systems Gmbh, DMC has 33 total recalls tracked by RecallDetector.

Related Recalls

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