RecallRadar

FDA Drug recall D-0249-2026

Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-51…

On 2026-01-14 the FDA classified a Class II recall of Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-51… by Imprimis Njof, citing presence of particulate matter - Glass like particles.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0249-2026
ClassificationClass II
Statusongoing
Initiated2025-12-18
Published2026-01-14
Last updated2026-09-13 11:52 UTC
CompanyImprimis Njof
DistributionUS

Product

Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-512-0.1

Reason

Presence of particulate matter - Glass like particles.

Identifiers

code_infoLot: 25MAY051, Expires: 06/26/2026; 25AUG003, Expires:08/07/2026

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0249-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.