Lantheus MI Radipharmaceuticals Inc. recalls Fludeoxyglucose F 18 Injection, 20mCi/mL to 200 mCi/mL at EOS, 30 mL Multiple-Dose Vial, Rx Only, Manufactured by: Lanth
Recalled July 12, 2017 · FDA recall D-0942-2017 · Lantheus MI Radipharmaceuticals
Hazard
Failed Impurities/Degradation Specifications; out of specification result for Acetonitrile residual solvent · FDA Class III
Units
26 doses
Sold at
Puerto Rico
Description
Failed Impurities/Degradation Specifications; out of specification result for Acetonitrile residual solvent
Product
Fludeoxyglucose F 18 Injection, 20mCi/mL to 200 mCi/mL at EOS, 30 mL Multiple-Dose Vial, Rx Only, Manufactured by: Lantheus MI Radiopharmaceuticals, Inc., San Juan, PR --- NDC 11994-015-01
Manufacturer(s)
Lantheus MI Radipharmaceuticals Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →