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FDA Orders Recall on Diabetes App After Glitch Injures 224 Users

FDA Orders Recall on Diabetes App After Glitch Injures 224 Users
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Drug administrationTandem diabetes careOzempic crazePeople buyingDiabetic medClassi recallClosely monitor pumpUrgent medical device correction

FDA Warns About Impella Left-Sided Blood Pumps, Linked to 49 Deaths

FDA issued a warning for the the Impella left-sided blood pumps as it had received many reports of heart-wall tears, increasing the risk of death, hypertension, and more.

United statesNew yorkJohnson medtechRitaf redbergSethd bilazarianAbiomed incUniversity of californiaNew york timesDrug administrationUrgent medical device correctionImpella left sided blood pumpsAccessed marchClassi recallAll left sided impellaPump is linkedAcute myocardial infarction complicated

Fresenius Medical Care recalls 12M syringes

Fresenius Medical Care is recalling more than 12 million syringes due to reports of blood or heparin leaking and

Fresenius medical careMedical careSanxin single use sterile syringesLuer lockClassi recallAnxin single use syringes0 milliliter luer lock0 milliliter luer lock

Abbott Medical recalling Proclaim spinal cord stimulators following 73 injuries

FDA has issued a Class I recall of 155,028 Abbott Medical implantable neurostimulation systems due to an inability to exit MRI mode, potentially leading to seri

Abbott medicalAbbott proclaimAbbott julyProclaim plusClassi recallAbbott medicalRoclaim neurostimulation systemsElectrical impulsesErve structuresSpinal cord stimulationProclaim xrRoclaim plus 5Roclaim plus 7Roclaim drg

13K ventilator parts pulled in Class I recall

Mallinckrodt Manufacturing has recalled 13,600 one-way valves made for ventilators because of a possible risk of serious injury or death.

Mallinckrodt manufacturingNe way valvesClassi recallSerious injury

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