Recalls

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

FDA issued recall of Silver Bullet 10x by Nature’s Rx due to undeclared PDF-5 inhibitors.

FDA issued recall of VentStar and ID Breathing Circuits and Anesthesia Sets by Draeger Medical due to possible incorrect assembly.

FDA issued recall of irbesartan and irbesartan/hydrochlorothiazide (HCTZ) tablets by Prinston Pharmaceutical due to NDEA impurity.

FDA issued recall of Synergy Cranial software and Stealth Station S7 Cranial software by Medtronic due to inaccuracies displayed during surgical procedures.

FDA issued recall of Rhino 5k capsules by Happy Together due to presence of undeclared sildenafil and tadalafil.

FDA issued recall of vecuronium bromide for injection by Sun Pharmaceutical Industries due to particulate matter.

FDA issued recall of ceftriaxone for injection by Lupin Pharmaceuticals due to particulate matter.

FDA issued recall of losartan potassium tablets, USP by Torrent Pharmaceuticals Limited due to impurity.

FDA issued recall of CAmlodipine/Valsartan Tablets USP, Valsartan/HCTZ Tablets, USP and Valsartan Tablets USP by Aurobindo due to NDEA (N-Nitrosodiethylamine) impurity.