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Teleflex Recalls Arrow Intra-Aortic Balloon Pumps for Short Battery

Arrow International, LLC, a Subsidiary of Teleflex, Inc, recalls Arrow AutoCAT 2, AC3 intra-aortic balloon pumps for unexpectedly short battery run times

Emergency departmentTeleflex incRoom serviceDrug administrationVascular access serviceCatheter labTeleflex customer serviceHarrow internationalAortic balloonRecall databaseArrow intra aortic balloon pumpsAortic balloon pumpsUrgent medical device notificationAcknowledgement formTeleflex customer

Medtronic Recalls HeartWare HVAD System Batteries Due to Battery Failure

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Medtronic incMedtronic patient servicesDrug administrationRecall databaseHeartware ventricular assist devicePower disconnectAlarm logUrgent medical device correctionMedtronic field representativeCustomer confirmation form

Class I Recall of Percutaneous Thrombolytic Device

Arrow-Trerotola over-the-wire 7FR PTD kits are being recalled because the orange inner lumen of the catheter s tip may separate from the basket causing injury.

United statesArrow international incDrug administrationRecall databasePatient safetyThrombolytic therapyImplanted device cardiologyUs food and drug administrationNited states food and drug administrationBlood vesselsVascular accessKidney dialysisRenal dialysisWound managementArteriovenous fistula

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