Philips Issues New Urgent Medical Device Correction for Ventilators
Philips Respironics issued an Urgent Medical Device Correction Letter regarding a problem for certain ventilators that could harm patients.
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Search Results for: philips recall
FDA Class I Recalls Hit 15-Year High in 2022
Sedgwick released its 2023 Product Recall Index, which detailed why defective and violative products reached a record-breaking high.
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Reworked Philips Ventilators Get Class I Recall for Potential Foam Debris Issues
Philips Respironics recalled certain reworked ventilators for issues related to foam adhesion failure and foam debris.
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Philips CPAP Recall Spurs Another 82 Reports of Patient Deaths, Pushing Total to 346
Recent medical device reports regarding Philips’ CPAP machines registered additional fatalities, expanding the number of reported deaths.
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Philips Respironics Ventilators Get New FDA Recall Notice
The FDA is providing additional information to patients, caregivers, and healthcare providers about two recent issues in certain ventilators.
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