Mckesson Medical-Surgical recalls Systane Zaditor eye drops (0.035% ketotifen fumarate) because they were stored outside label specifications. This may affect product safety.
CGMP Deviations: products were stored outside the drug label specifications.
Mckesson Medical-Surgical is recalling Systane Zaditor eye drops that were stored outside the required drug label specifications. This could lead to improper product safety.
The eye drops were stored outside the drug label specifications, which could affect their safety and effectiveness. This may lead to improper product performance or potential harm.
People who purchased Systane Zaditor eye drops (0.035% ketotifen fumarate) from pharmacies or online retailers. Those with sensitive eyes or allergies may be at higher risk.
Check for the product name 'Systane Zaditor' or 'Ketotifen fumarate ophthalmic solution 0.035%'. The NDC code 0065-4011-05 is also listed on the bottle.
Look for the NDC code 0065-4011-05 on the bottle label to confirm if the product is recalled.
The recall indicates the product was stored outside label specifications, but the official notice does not specify if it is safe to use.
Check for the NDC code 0065-4011-05 on the bottle label or look for the product name 'Systane Zaditor'.
The official notice does not provide specific action steps for the recalled product.
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-1317-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1317-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
