Infusion Options, Inc. recalls PEMETREXED 910 MG QS 100 ML NS IVPB; PEMETREXED 940 mg QS 100 ml NS IVPB; PEMETREXED 1000 mg QS 100 ml 0.9% NACL IVPB;
Recalled August 21, 2019 · FDA recall D-1803-2019 · 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
PEMETREXED 910 MG QS 100 ML NS IVPB; PEMETREXED 940 mg QS 100 ml NS IVPB; PEMETREXED 1000 mg QS 100 ml 0.9% NACL IVPB; PEMETREXED 490 MG /100 ml NS IVPB; PEMETREXED 800 mg/ 100 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 →