Avanos Medical Recalls Closed Suction Systems for Young Children
The FDA has identified Avanos Medical’s recall of certain airway access devices for children, infants, and neonates as a Class I recall
Read MoreThe FDA has identified Avanos Medical’s recall of certain airway access devices for children, infants, and neonates as a Class I recall
Read MoreApr 18, 2023 | Recalls, Ventilators | 0 |
The recall addresses potential risks that glued connections of breathing circuits may loosen either before or during the ventilation process.
Read MoreApr 12, 2023 | FDA Updates, Patient Care Equipment | 0 |
Avation Medical announced that its non-invasive, bladder control therapy device, Vivally, received U.S. FDA 510(k) clearance.
Read MoreApr 5, 2023 | Ventilators | 0 |
Philips Respironics issued an Urgent Medical Device Correction Letter regarding a problem for certain ventilators that could harm patients.
Read MoreMar 21, 2023 | Infusion Therapy | 0 |
The reduction in duration of hospital stays and cost-of-care is driving growth of the home infusion therapy market.
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