Draeger Issues Recall Notification for Certain Breathing Circuits
The recall addresses potential risks that glued connections of breathing circuits may loosen either before or during the ventilation process.
The recall addresses potential risks that glued connections of breathing circuits may loosen either before or during the ventilation process.
Early on during the pandemic, the state of New York spent millions of dollars on equipment that was aimed at aiding COVID patients, much of which is currently dormant and with no plans to be used.
Philips may be looking to bring an end to its ongoing plight of medical device recalls via a settlement agreement with the DOJ.
The recall addresses potential risks that glued connections of breathing circuits may loosen either before or during the ventilation process.
The FDA updated a safety communication regarding medical device reports associated with the breakdown of materials used in Philips devices.
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Read MoreThe FDA is proposing an order be issued that would require Philips Respironics to address recalled devices, including millions of ventilators.
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Read MorePhilips is facing another string of recalls in its portfolio, which have a received a Class I rating, the most serious type of recall.
Read MoreAmid an ongoing current of medical product recalls, hospitals in the United Kingdom are experiencing new electrical problems with certain Philips ventilators.