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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

Imprimis NJOF, LLC 2025-07-30 Health moderate FDA
Health · FDA · Recall #FDA-D-0536-2025

Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5%… Recall

Issued July 30, 2025 · Imprimis NJOF, LLC

In July 2025, Imprimis NJOF, LLC recalled the Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5%…, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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

What you should do

  1. 1 Stop using Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5%… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Imprimis NJOF, LLC to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Imprimis NJOF, LLC
Category
Health
Recall date
July 30, 2025
Units affected
Not reported
Sold at
Nationwide in the USA
Recall number
FDA-D-0536-2025
Made in
United States
Issuing agency
FDA

In context

  • Imprimis NJOF, LLC has 9 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 691st Health recall we've logged in 2025.
Read the official FDA notice

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