Medline Recalls Sub-G Endotracheal Tube for Choking Risk
Medline recalled the Sub-G Endotracheal Tube with Subglottic Suction due to risks of detachment, tearing, and potential airway obstruction.
Read MoreMedline recalled the Sub-G Endotracheal Tube with Subglottic Suction due to risks of detachment, tearing, and potential airway obstruction.
Read MoreAbbott is recalling the HeartMate 3 LVAS due to issues with blood leakage and air entrapment during implantation.
Read MoreTruAsset has integrated with Equiptrack to enhance the efficiency of processing FDA recalls and streamline patient safety processes.
Read MoreOptumHealth Care Solutions is recalling Nimbus II Plus infusion pumps due to multiple failure modes, following an InfuTronix recall.
Read MoreU.S. product recalls increased by 8% in the first quarter of 2024, with the medical device industry seeing a 13.8% surge in recalls.
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