Mckesson recalls Systane lubricant eye drops due to improper storage conditions. Products may not meet drug label specifications. Consumers should check NDC codes and contact Mckesson for details.
CGMP Deviations: products were stored outside the drug label specifications.
Mckesson is recalling Systane lubricant eye drops because they were stored outside drug label specifications. This could mean the product doesn't meet safety standards, but the recall doesn't specify immediate harm or injury.
The product was stored outside the required drug label specifications, which could affect its safety and effectiveness. This means the drops might not work as intended or could pose a risk if not handled correctly.
People who own or use Systane lubricant eye drops with NDC codes 0065-0429-15 or 0065-0429-30 are affected. Those with dry eyes may be at slightly higher risk if the product is not stored properly.
Check for NDC codes 0065-0429-15 (15 mL) or 0065-0429-30 (30 mL) on the bottle. The product is labeled as Systane lubricant eye drops from Alcon Surgical Inc.
Look for NDC codes 0065-0429-15 or 0065-0429-30 on the bottle label.
The recall states the product was stored outside drug label specifications, but it does not say the product is unsafe or has caused injuries. Consumers should check the NDC codes and contact Mckesson for details.
The recall does not specify a remedy, so no action is required beyond checking the NDC codes. Contact Mckesson for further instructions if needed.
Check for NDC codes 0065-0429-15 (15 mL) or 0065-0429-30 (30 mL) on the bottle label.
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-1314-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1314-2022 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.
