FDA labetalol recall

May 23, 2014

HOSPIRA will initiate a voluntary nationwide recall to the user level for one lot of labetalol hydrochloride injection, USP, 100 mg/20 mL (5 mg/mL) 20 mL multidose vial. The recall is due to embedded particulate within the glass vial and visible particles floating in the solution; the embedded particulate was identified as stainless steel and the visible particles as iron oxide. There is no evidence of this fault affecting Australian supplies. For more, CLICK HERE.

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Pharmacy Daily | FDA labetalol recall

FDA labetalol recall

Other recent headlines

LGP results set it for growth

On-site experts in aged care facilities

Pharmacist invention seeks US patent

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES