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Recall archive

95,388 stored notices, from Jun 20, 2012 to Nov 11, 2026.

101 recalls · page 5 of 5

Medical devices

Reported Dec 16, 2020

Philips IntelliVue X2 Multi measurement Server: M3002A (865039) - Product Usage: intended for monitoring and recording…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

Matched: Brand · Product · Product details — Speakers on IntelliVue X2 and IntelliVue MP2 may fail, identified by the display of a Speaker Malfunct. INOP or by the absence of audible sound, may…

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2020

Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

Matched: Brand · Product · Product details — Affected devices contain a Printed Circuit Assembly (PCA) that was not manufactured/repaired in accordance to quality standards.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 2, 2019

Philips HeartStart Infant/Child SMART Pads Cartridge, Model # M5072A, UDI:00884838023758

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

Matched: Brand · Product · Product details — The recall is being initiated due to incorrect age range labeling (8+ yrs) on the foil packaging for infant/child pad cartridges. The infant/child…

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2018

HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

Matched: Brand — Affected lithium-ion batteries may contain a defective component (Thermal Cut-off or TCO). Should the component fail, the battery will no longer…

FDA (openFDA device enforcement)

Medical devices

Reported Feb 28, 2018

Philips QCPR Meter - used with FR3 Product Usage: The Philips CPR meter is intended for use with the Philips HeartStart…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Electronics North America Corporation

Matched: Brand · Product · Product details · Reason for recall — Inform users of correct placement of the disposable adhesive pad on the QCPR meter and inform users of injuries associated with proper performance of…

1 more product in this recall

FDA (openFDA device enforcement)

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