Recalls

FDA issued recall of Spine & Trauma 3D Navigation by Brainlab AG due to inaccurate display.

FDA issued recall of aphrodisiac capsules by SD Import due to undeclared sildenafil.

FDA issued recall of o_two e700, e600 and e500 automatic transport ventilators by O-Two Medical Technologies due to fire risk.

FDA issued recall of DG/Health NATURALS baby cough syrup + mucus by Kingston Pharma due to possible health risk.

FDA issued recall of BLUEFUSION capsules by Ata Int. due to undeclared ingredients.

FDA issued recall of levoleucovorin injection by Mylan Institutional due to particulate matter.

FDA issued recall of Transseptal Needle by Cook Medical due to risk of plastic fragments.

FDA issued recall of 8.4% sodium bicarbonate injection by Hospira due to particulate matter.

FDA issued recall of Losartan Potassium Tablets by Legacy Pharmaceutical Packaging due to impurity.

FDA issued recall of Raindrop Near Vision Inlay by RVO 2.0 due to corneal haze.

FDA issued recall of Kratom products by Sunstone Organics due to salmonella.

FDA issued recall of drospirenone and ethinyl estradiol tablets by Apotex Corp due to missing/Incorrect tablet arrangement.

FDA issued recall of LIFEPAK15 by Physio-Control due to risk of device failure.

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.

FDA issued recall of Infants’ Ibuprofen Concentrated Oral Suspension by Tris Pharma due to potential higher concentrations of ibuprofen; three additional lots added.