Subpotent Drug; sub-potent Bromfenac levels, below the 90.0-110.0% specification range.
Subpotent Drug; sub-potent Bromfenac levels, below the 90.0-110.0% specification range.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Imprimis NJOF, LLC to request your refund or repair — edit it as you like.
Subject: Recall D-1094-2023 — Imprimis NJOF, LLC Imprimis NJOF, LLC recalls Moxifloxacin - Bromfenac Sterile Ophthalmic Solution Hello, I own a Imprimis NJOF, LLC recalls Moxifloxacin - Bromfenac Sterile Ophthalmic Solution 0.5% / 0.075%, 5mL bottle, Imprimis NJOF, LLC. 1705 Route 46 West, that is covered by recall D-1094-2023 from Imprimis NJOF, LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
