Fagron recalls 0.5mL single-use eye drop solution due to incorrect product formulation. This may affect safety if used improperly. Contact Fagron for details.
Incorrect Product Formulation
Fagron is recalling a specific eye drop solution because it was made with the wrong ingredients. Using this product could cause harm if it's not used correctly.
The product was formulated incorrectly, meaning it contains the wrong mix of ingredients. This could lead to unsafe effects if used as intended for eye treatment.
People who have purchased this eye drop solution for eye use are affected. Those with eye conditions requiring medication are at higher risk.
Check for the product name 'Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic Solution' on the label. The NDC number 71266-8240-01 and lot number C274-000047958 are also indicators.
Look for the product name and NDC number 71266-8240-01 on the label.
The recall states the product has an incorrect formulation, so it may not be safe. Do not use it until you contact Fagron.
Check for the product name and NDC number 71266-8240-01 on the label.
The recall does not specify a remedy, so contact Fagron directly for instructions.
We’ve drafted a message you can send Fagron to request your refund or repair — edit it as you like.
Subject: Recall D-0221-2026 — Fagron Fagron Hello, I own a Fagron that is covered by recall D-0221-2026 from Fagron. 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.
