Fresenius Kabi USA, LLC recalls OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius K
Recalled June 1, 2016 · FDA recall D-0866-2016 · Fresenius Kabi USA
Hazard
Failed Impuities/Degradation Specifications · FDA Class II
Units
355,150 vials
Sold at
Nationwide and Puerto Rico.
Description
Failed Impuities/Degradation Specifications
Product
OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-01.
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →