FDA Proposes Order Forcing Philips to Repair, Replace or Refund All Recalled Ventilators
The FDA is proposing an order be issued that would require Philips Respironics to address recalled devices, including millions of ventilators.
Read MoreMay 5, 2022 | FDA Updates, Ventilators | 0 |
The FDA is proposing an order be issued that would require Philips Respironics to address recalled devices, including millions of ventilators.
Read MoreApr 29, 2022 | Recalls, Ventilators | 0 |
Covidien, LP is recalling its Puritan Bennett 980 Series Ventilator due to a capacitor manufacturing assembly error.
Read MoreApr 26, 2022 | Ventilators | 0 |
Allendale, N.J.-based Solutions in Critical Care announces that it has entered into a long-term agreement to carry Inovytec’s Ventway Sparrow EMS and MRI ventilators.
Read MoreApr 22, 2022 | Patient Safety, Ventilators | 0 |
Earlier this week, the U.S. FDA revealed that the Philips’ Respironics V60 ventilator received a Class 1 recall due to an electrical circuit fault that can use the device to malfunction. Now, Philips is investigating one patient death and four reports of patient harm possibly related to the recall.
Read MoreApr 20, 2022 | Recalls, Ventilators | 0 |
Philips is facing another string of recalls in its portfolio, which have a received a Class I rating, the most serious type of recall.
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