Recall archive
5 recalls · page 1 of 1
Reported Sep 8, 2021
CombiDiagnost R90 Software Version R1.0 and R1.1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
Matched: Brand · Reason for recall — Philips has become aware of a software issue, where the kV and mA values are not locked immediately but change when the collimator shutter position…
FDA (openFDA device enforcement)
Reported Feb 26, 2020
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
Matched: Brand · Product · Product details · Reason for recall — When using the Table Up/Down button, the system may experience Error 80, which locks the geometry in that specific state, requiring the intervention…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
Matched: Brand · Product · Product details — kV/mA lockin not functioning as specified which may result in the patient receiving an increased radiation dose.
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
Matched: Brand · Product · Product details · Reason for recall — Stitching run on SkyPlate detector interrupted intermittently; Stitching with SkyPlate aborts after first image; System software CD contains wrong…
FDA (openFDA device enforcement)
Reported Aug 29, 2018
DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
Matched: Brand — The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or…
27 more products in this recall
FDA (openFDA device enforcement)
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