D-0535-2025 Class II Ongoing

Recalled by Imprimis NJOF, LLC — Ledgewood, NJ

Recall Details

Product Type
Drugs
Report Date
July 30, 2025
Initiation Date
July 9, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
6,880 vials

Product Description

Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01

Reason for Recall

Sub-Potent Drug: Subpotent assay results during stability testing.

Distribution Pattern

Nationwide in the USA

Code Information

Lot: 24DEC017, Exp. 07/12/2025.