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Draeger Issues Recall Notification for Certain Breathing Circuits

Apr 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.

Avation Medical announced that its non-invasive, bladder control therapy device, Vivally, received U.S. FDA 510(k) clearance.

Apr 5, 2023 | Ventilators | 0 |

Philips Respironics issued an Urgent Medical Device Correction Letter regarding a problem for certain ventilators that could harm patients.

Mar 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.

Getinge subsidiary Datascope is recalling two types of Intra-Aortic Balloon Pumps due to the possibility of unexpected device shutdown.