Mckesson Medical-Surgical recalls Tropicamide Ophthalmic Solution 1% 3mL bottles due to temperature abuse risks. This prescription medication may be unsafe if stored improperly.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Tropicamide Ophthalmic Solution 1% 3mL bottles because they were manufactured with temperature abuse risks. This means the medication could be unsafe if stored incorrectly.
The medication was produced with temperature abuse risks, meaning it could be unsafe if stored improperly. This is a manufacturing issue that affects the product's safety.
Prescription patients who received this medication from a pharmacy. Those who have the specific product with NDC 6131435502 are most at risk.
Check for the 3mL bottle labeled Tropicamide Ophthalmic Solution 1% with NDC 6131435502. The product was distributed by Mckesson Medical-Surgical and requires a prescription.
Look for the NDC code 6131435502 on the bottle label to confirm if it's recalled.
The recall indicates potential temperature abuse risks, but the official notice doesn't specify if it's safe to use.
Check for the NDC code 6131435502 on the bottle label. This product was distributed by Mckesson Medical-Surgical and requires a prescription.
The official notice doesn't specify a remedy, so contact your pharmacy or healthcare provider for guidance.
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-1108-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1108-2022 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.