RRD Simplifies Medical Device Recall Notification Process
RRD’s solution aims to ensure end-to-end support throughout the complex recall notification process for medical device companies.
Read MoreRRD’s solution aims to ensure end-to-end support throughout the complex recall notification process for medical device companies.
Read MoreFresenius Kabi has issued a voluntary recall of the Ivenix Infusion System due to a leak in the system that allows fluid to enter the administration set loading area near the air detector.
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 MoreMar 17, 2023 | Patient Care Equipment, Patient Safety, Recalls | 0 |
Getinge subsidiary Datascope is recalling two types of Intra-Aortic Balloon Pumps due to the possibility of unexpected device shutdown.
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