Recall of drospirenone and ethinyl estradiol tablets, USP, 3 mg/ 0.02mg by Jubilant Cadista Pharmaceuticals due to out of specification (OOS) dissolution results.
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Recall of all drug products by Herbal Doctor Remedies due to marketing without FDA approval and concerns with manufacturing practices.
Recall of intra-aortic balloon pumps by Maquet/Datascope due to potential battery failure.
Recall of Kogenate FS antihemophilic factor (recombinant) by Bayer due to mislabeled drug vial.
Recall of Alaris pump model 8100 infusion sets by Becton Dickinson due to faster than expected delivery of medication.
Recall of neonatal ConchaSmart Breathing Circuit by Teleflex due to circuit cracks.
Altaire issued the retail level recall over quality concerns at their manufacturing facility.
Recall of Giraffe infant warmers and Panda i-Res infant warmers by GE Healthcare due to bedside panels and latch areas cracking or breaking.
Recall of Hamilton-G5 ventilators by Hamilton Medical AG due to error message.
Recall of multiple ophthalmic products by Altaire Pharmaceuticals due to potential for nonsterility.
Recall of fluorouracil injection by Fresenius Kabi USA due to potential for glass particulate.
Recall of SmartSite syringe administration set by Becton Dickinson & Company (BD) due to risk of leaks.
Recall of IntraClude intra-aortic occlusion device by Edwards Lifesciences due to risk of balloon rupture.
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