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Recall archive

94,355 stored notices, from Jun 20, 2012 to Sep 23, 2026.

8 recalls · page 1 of 1

Medical devices

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 detailsCertain 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)

Medical devices

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 recallPhilips has discovered through customer complaints and internal testing an intermittent electronic product defect in accordance with 21 CFR…

FDA (openFDA device enforcement)

Medical devices

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 detailsMagnet 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)

Medical devices

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 detailsAdditional 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)

Medical devices

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 recallThere 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)

Medical devices

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: BrandDuring automatic tabletop movement, pressing and holding the Stop Table button may lead to an unexpected restart of the table movement.

FDA (openFDA device enforcement)

Medical devices

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 recallThe 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)

Medical devices

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 recallThe 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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