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FDA recall 99756: ImprimisRx NJ LLC: Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution

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FDARecall 99756Medicines

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

Subpotent Drug
Text from FDA, unedited.

FDA classification: Class III. Use is not likely to cause adverse health consequences. Status: Ongoing.

Is it yours? Products and codes

  • Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10

    Lot or code
    Lot #: 26JAN035, BUD 09/07/2026; 26FEB015, BUD 09/24/2026
    FDA recall number
    D-0835-2026
    Quantity
    772 bottles

Distribution (FDA): USA Nationwide

About this record

Issued by
U.S. Food and Drug Administration
Firm
ImprimisRx NJ LLC
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “Subpotent Drug”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

When was this recall published?

FDA published recall 99756 on September 16, 2026.

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