Attention Members: Manufacturer recall of Fluorouracil Injection
Manufacturer Fresenius Kabi is voluntarily recalling two lots of Fluorouracil Injection USP, 5g/100mL (50mg/mL), 100mL fill in a 100mL vial due to potential contamination of the medicine with glass particles. On July 24, 2019, the Food and Drug Administration (FDA) stated that this is a Class I Recall.
We want to make sure you have the information you need to take care of your health. Please discuss this with your doctor at your next visit.
To date, Fresenius Kabi has not received any complaints or reports of adverse events related to this recall. For more information, please visit www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/fresenius-kabi-issues-voluntary-nationwide-recall-two-lots-fluorouracil-injection-due-potential. You can also call Horizon NJ Health Pharmacy Help Desk at 1-800-682-9094 (TTY 711) x81016 , Monday through Friday, 8 a.m. to 6:30 p.m. and Saturday 8 a.m. to 4:30 p.m., Eastern Time.