Mckesson Medical-Surgical recalls Naphcon A eye drops and antihistamine eye drops because they were stored outside drug label specifications. Consumers should check product labels for NDC 0065-0085-15.
CGMP Deviations: products were stored outside the drug label specifications.
Mckesson Medical-Surgical is recalling Naphcon A eye drops and antihistamine eye drops that were stored outside the required drug specifications. This could lead to improper medication effectiveness or safety issues if the product was not stored correctly.
The eye drops were stored outside the drug label specifications, which could affect their effectiveness or safety. This is a manufacturing issue related to storage conditions, not a direct hazard like a chemical reaction or physical damage.
People who own or use these eye drops, especially those who have the specific NDC number 0065-0085-15. The risk is low as the hazard relates to storage conditions rather than immediate harm.
Check for the product name 'Naphcon A eye drops' or 'Redness Reliever and Antihistamine Eye Drops' with NDC number 0065-0085-15. The product comes in 15 mL bottles from Alcon, a Novartis company.
Look for the NDC number 0065-0085-15 on the bottle to confirm if it is recalled.
The recall is due to improper storage conditions, not the product being unsafe when used correctly. The hazard is related to storage, not immediate harm.
Check for the NDC number 0065-0085-15 on the bottle, which is specific to this recall.
The recall does not require discarding the product; checking the label is sufficient to determine if it is recalled.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1313-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1313-2022 from Mckesson Medical-Surgical. 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.
