News: Recalls

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.

Recall of enFlow fluid warming system disposable cartridges by Vyaire Medical due to risk of elevated aluminum level exposure to patients.

Recall of Hudson RCI Sheridan and Sheridan Endotracheal Tubes by Teleflex Medical due to connector disconnecting from the breathing circuit.

Recall of unexpired sterile drug product lots by Infusion Options Inc. due to lack of sterility assurance.

Recall of unexpired sterile drug product lots by RXQ Compounding, LLC (“RXQ”) due to lack of sterility assurance.

Recall of unexpired sterile drug product lots by Premier Pharmacy Labs due to lack of sterility assurance.

Recall of Advance Enforcer 35 Focal-Force PTA balloon catheter 6mm x 4cm by Cook Medical due to balloons bursting below the rated burst pressure.

Recall of losartan potassium to 50 mg and 100 mg tablets USP by Teva Pharmaceuticals USA due to impurity.

Recall of Candy King - Worms 3 mg 100 mL by Drip More due to elevated nicotine.

Recall of PECGEN DMX by NOVIS PR due to labeling error.

Recall of SOLOPATH Balloon Expandable TransFemoral System and Re-Collapsible Balloon Access System by Terumo Medical Corporation due to dislodgement of the fairing tip from the sheath.

Recall of amikacin sulfate injection, USP 1gm/4 mL (250mg/mL) and prochlorperazine edisylate injection, USP 10mg/2mL (5mg/mL) by Heritage Pharmaceuticals due to sterility test failure.

Recall of veterinary products by Norbrook Laboratories Limited due to potential lack of sterility.