FDA recall D-0410-2022

Edge Pharma, LLC · Class II · drug

Product

Moxifloxacin, Sterile Ophthalmic Solution for Injection, Preservative Free, 0.8mg/0.8 mL (1mg/mL), 0.8 mL per syringe, Single Use Syringe, For Intraocular Injection, Edge Pharma, LL, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1050-01

Reason for recall

Lack of Assurance of Sterility

Distribution

nationwide

Key facts

Status
Terminated
Initiation date
2021-12-06
Report date
2022-02-02
Termination date
2023-06-07
Voluntary/Mandated
Voluntary: Firm initiated
Location
Colchester, VT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0410-2022