Product Safety Recalls

Product Recall Tracker

Recall D-0299-2022

Description: Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, NDC 61958-2901-2

Recall D-0299-2022 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberD-0299-2022
Event ID89153
DistributionNationwide in the USA
Quantity53,473 vials
Recall ReasonPresence of Particulate Matter: investigation into a customer complaint confirmed the presence of glass particulates.
Drug ClassificationClass I
Drug Code Info20220105
Recall Initiation Date20211203
Report Date20220105
Classification Date20211228
Address333 Lakeside Dr
Foster City, CA 94404-1147
United States
Recalling FirmGilead Sciences, Inc.
Initial Notification Press Release
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.