Infusion Options, Inc. recalls RAMUCIRUMAB 457 MG QS 250 ML NS IVPB; AMUCIRUMAB 1182 MG QS 250 ML NS IVPB; Rx Only, Infusion Options, Inc. 5924 13the A
Recalled August 21, 2019 · FDA recall D-1807-2019 · Infusion Options
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
N/A
Sold at
NY only
Description
Lack of Assurance of Sterility
Product
RAMUCIRUMAB 457 MG QS 250 ML NS IVPB; AMUCIRUMAB 1182 MG QS 250 ML NS IVPB; Rx Only, Infusion Options, Inc. 5924 13the Ave, Brooklyn, NY 11219-4934, 718-283-7233
Manufacturer(s)
Infusion Options, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →