Recall archive
8 recalls · page 1 of 1
Reported Jun 30, 2021
Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028, 722029,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand · Product · Product details — Certain low-voltage DC power supplies (DCPS) used in these products may be subject to an increased probability of failure. Failure of a DCPS may…
FDA (openFDA device enforcement)
Reported Aug 7, 2019
Azurion lnterventional Fluoroscopic X-ray System, with software version 1.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand · Product · Product details · Reason for recall — Philips has discovered through customer complaints and internal testing an intermittent electronic product defect in accordance with 21 CFR…
FDA (openFDA device enforcement)
Reported May 8, 2019
Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand · Product · Product details — Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks to personnel servicing the MED, MDD or…
FDA (openFDA device enforcement)
Reported Apr 24, 2019
Foot Switches used with Philips MultiDiagnost Eleva with Flat Detector; Product Codes: 708037, 708038 Product The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand · Product · Product details — Additional units have been identified for previous recall Z-1280-2016 (RES 69339): If a Footswitch is frequently used on a non-flat surface or in the…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Prodiva CS, Model Number 781069. Nuclear Magnetic Resonance Imaging System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand · Product · Product details · Reason for recall — There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
63 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 16, 2019
Ingenia Elition S, Ingenia Elition X
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand — During automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.
FDA (openFDA device enforcement)
Reported Jul 4, 2018
OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic, Product Nos. 708026, 708027, 708028
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand · Product · Product details · Reason for recall — The fixation of the upper and lower tilt actuator, of the Omnidiagnost system might break off and the table will start to rotate from 0 to + 90 /- 90…
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 9, 2018
MultiDim Eleva 708032 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederlands
Matched: Brand · Product · Product details · Reason for recall — The fixation of the upper and lower tilt actuator, of the MD-Eleva system might break off and the table will start to rotate from 0 to + 90 I- 90…
6 more products in this recall
FDA (openFDA device enforcement)
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