Recalled Ciprofloxacin eye drops (0.3% solution) may have been exposed to unsafe temperatures during shipping, risking reduced effectiveness. Contact your pharmacy for details.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Ciprofloxacin Ophthalmic Solution 0.3% eye drops due to potential temperature abuse during shipping. This could make the medication less effective than intended.
The medication may have been exposed to unsafe temperatures during shipping, which could reduce its effectiveness. This is a quality issue, not a safety hazard like causing injury.
Prescription eye drop users who received this specific product from a pharmacy. People with eye infections needing this medication are most at risk.
Check for the 10 mL bottle labeled 'Ciprofloxacin Ophthalmic Solution 0.3%, Rx only' with NDC 61314-0656-10. The product was distributed by Mckesson Medical-Surgical.
Look for the 10 mL bottle with NDC 61314-0656-10 and 'Ciprofloxacin Ophthalmic Solution 0.3%, Rx only' label.
No, this is a quality issue that may reduce effectiveness, not a safety hazard like causing injury.
Check for the 10 mL bottle labeled 'Ciprofloxacin Ophthalmic Solution 0.3%, Rx only' with NDC 61314-0656-10.
Contact your pharmacy for details about the specific product you received.
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-1029-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1029-2022 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.
