FDA recall D-0414-2022

Edge Pharma, LLC · Class II · drug

Product

Phenylephrine HCl / Tropicamide / Ciprofloxcin / Ketorolac Sterile Ophthalmic Solution, 10%/1%/0.3%/0.125%, 0.8 mL per syringe, Single Use Syringe, For Topical Ophthalmic Use, Edge Pharma, LLC, 856 Hercules Dr., Colchester, VT 05446, NDC 05446-1270-01

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-0414-2022