Is Latanoprost recalled?
Yes — there is an active recall. 2 ongoing FDA recalls mention Latanoprost (11 total). Check the affected lots below.
Most common reason: Chemical / undeclared (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Latanoprost. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Latanoprost recalls on record
none so far in 2026; 11 on record, newest firstXelpros (latanoprost ophthalmic emulsion)
Failed Release Testing: Out of specification for particulate matter test.
Timolol-Latanoprost
Subpotent Drug: The batches contain less than 90% of the labeled amount of latanoprost.
Timolol- Dorzolamide- Latanoprost P-F
Subpotent Drug
Timolol-Latanoprost P-F
Subpotent Drug
Timolol-Brimonidine-Dorzolamide-Latanoprost
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Timolol-Latanoprost PF Solution
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Latanoprost PF Solution
Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil was used due to a mislabeling by the supplier
Latanoprost Ophthalmic Solution
Lack of assurance of sterility: product was found to be empty, under-filled, or leaking.
Latanoprost Ophthalmic Solution
Lack of Assurance of Sterility: Failed at expiry for Preservative Effectiveness Test (PET), therefore the product may be susceptible to microbial growth before the expiry date.
Latanoprost 0.025% eye drop
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
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