FDA issued recall of DG/Health NATURALS baby cough syrup + mucus by Kingston Pharma due to possible health risk.
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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 a warning that tofacitinib (Xeljanz, Xeljanz XR) may increase the risk of pulmonary embolism in patients with rheumatoid arthritis.
FDA is strengthening warnings in the febuxostat (Uloric) product labeling and has added a Medication Guide requirement because of an increased risk of cardiovascular death and all-cause mortality.
Apotex Corp. voluntarily recalled drospirenone and ethinyl estradiol tablets.
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.
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