Mckesson Medical-Surgical recalls sterile eye drops due to temperature abuse during storage. Products may be unsafe if exposed to improper temperatures. Check your prescription label for NDC 6131462810.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling sterile eye drops that could be unsafe if stored at incorrect temperatures. This recall affects prescription products made by Sandoz with NDC 613:1462810. The hazard comes from temperature abuse during storage, which could lead to product instability.
The eye drops may become unstable if exposed to temperatures outside the recommended range during storage. This temperature abuse could lead to product degradation, potentially causing eye irritation or infection.
Prescription holders of Polymyxin B Sulfate and Trimethoprim Ophthalmic Solution, 10 mL bottles with NDC 6131462810. Patients using these eye drops for eye infections are most at risk if the product was stored improperly.
Check your prescription label for the NDC number 6131462810. The product is a sterile 0.1% eye drop solution, 10 mL bottle, made by Sandoz Pharma.
Look for the NDC number 6131462810 on the prescription label.
The product may be unsafe if stored at incorrect temperatures. Check the label for the NDC number 6131462810 to confirm if it's recalled.
Check the product label for the NDC number 6131462810. If it matches, contact your pharmacy for instructions.
The recalled product has the NDC number 6131462810 and is a sterile 0.1% eye drop solution, 10 mL bottle made by Sandoz Pharma.
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-1107-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1107-2022 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.
