Certain Draeger Medical Ventilators Get Class I Recall
Certain Draeger ventilators reportedly stopped ventilation because of a depleted battery, even after being re-connected to AC power.
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Johnson & Johnson Megadyne Electrodes Nab Class 1 Recall
The FDA has labeled the recall of two types of Megadyne electrodes manufactured by Johnson & Johnson’s Ethicon as a class I, the most serious.
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Asimily, HANDLE Partner for Healthcare Capital Management Cybersecurity
The new integration of Asimily with CCM provides a single platform for viewing all internet-connected assets to determine which assets or manufacturers are at risk of cybersecurity issues.
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FDA: Philips Ventilator Recall Report Numbers Increasing
The FDA received an additional 6,000 medical device reports January 1, 2023-March 31, 2023, related to PE-PUR foam used in Philips ventilators and other devices recalled in June 2021.
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Infusion System Replacement Batteries Get FDA Class I Recall
These infusion system replacement batteries were recalled because a defect has diminished how long they can be used to run the system, which may cause the system to shut down an ongoing infusion.
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