FDA recall D-0040-2024

Imprimis NJOF, LLC · Class III · drug

Product

Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular injection Preservative Free NDC 71384-640-01 Not for resale. Office use only. Lot: 23APR018 Date Compounded: 24APR2023 Expires on: 17APR2024. In case of adverse event contact: www.fda.gov/medwatch or (800)-FDA-1088 Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B, Ledgewood, NJ, 07852 (844) 446-6979

Reason for recall

Subpotent: Failing Test Results for Epinephrine

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2023-10-03
Report date
2023-10-11
Termination date
2025-03-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Ledgewood, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0040-2024