FDA issued recall of LIFEPAK15 by Physio-Control due to risk of device failure.
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FDA issued recall of GoLean Detox capsules by GoLean Detox USA due to undeclared ingredients.
FDA issued recall of losartan potassium/hydrochlorothiazide tablets, 100mg/25mg by Macleods Pharmaceuticals due to NDEA impurity.
FDA issued recall of ChemoLock Vial Spike by ICU Medical due to particle risk.
FDA issued recall of dual chamber implantable pulse generators by Medtronic due to circuit error.
FDA issued recall of levetiracetam in 0.54% sodium chloride injection 1500mg/100mL by Dr. Reddy's Laboratories due to mislabeling.
FDA issued recall of Swan-Ganz thermodilution catheter by Edwards Lifesciences due to incorrect assembly.
FDA issued recall of sterile saline and sterile water for inhalation by Medex Cardio-Pulmonary, doing business as Smiths Medical due to potential exposure to infectious agents as a result of...
FDA issued recall of LIFEPAK® 15 monitor/defibrillator by Stryker due to lock up after a defibrillation shock is delivered.
FDA issued recall of CoaguChek XS PT Test Strips by Roche Diagnostics due to inaccurate test results.
FDA issued recall of Vial2Bag fluid transfer systems by West Pharmaceutical Services due to potential malfunctions.
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