FDA Hands Philips its 5th Class I Recall of the Year for Faulty Ventilators
Philips’ recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.
Read MoreSep 28, 2022 | Patient Care Equipment, Recalls | 0 |
Philips’ recent recall regarding certain BiPAP machines has been classified as a Class I recall, according to the U.S. FDA.
Read MoreSep 20, 2022 | Patient Care Equipment | 0 |
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.
Read MoreSep 9, 2022 | Recalls, Ventilators | 0 |
Philips’ ventilator recall woes, which stemmed from the machines causing patient health issues, are under investigation by French prosecutors.
Read MoreSep 7, 2022 | Patient Care Equipment, Recalls | 0 |
Philips has recalled certain masks used with bilevel positive airway pressure machines and CPAP machines due to a serious safety concern.
Read MoreSep 2, 2022 | Medical Equipment, Patient Safety | 0 |
Philips RS North America a manufacturer of durable medical equipment agreed to pay over $24 million to resolve False Claims Act allegations.
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