Mckesson Medical-Surgical recalls Miocol-E eye drops due to temperature abuse risks. Affected products were distributed between June 1 and September 30, 2021. Consignees must check inventory records to determine if they received impacted products.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls Miocol-E eye drops (20 mg/2mL) because they may have been exposed to improper temperatures. This could cause the medication to become unsafe for use, though the recall focuses on specific distribution dates and inventory checks rather than immediate harm.
The medication may have been exposed to temperatures outside the safe range during distribution, which could affect its stability. This temperature abuse risk does not cause immediate harm but could lead to ineffective treatment if the medication is used improperly.
Healthcare facilities that received Miocol-E eye drops from Mckesson Medical-Surgical between June 1 and September 30, 2021. Patients using the medication under a prescription are not directly affected by this recall.
Check if your facility received Miocol-E eye drops (20 mg/2mL) from Mckesson Medical-Surgical between June 1 and September 30, 2021. The product is labeled with NDC 24208-539-20 and requires a prescription.
Use your facility's records to determine if you received Miocol-E eye drops between June 1 and September 30, 2021.
No. The recall requires checking inventory records to see if you received affected products between June 1 and September 30, 2021. There is no immediate action needed for users.
Contact Mckesson Medical-Surgical or Sedgwick for guidance on handling the product if you received it during the specified timeframe.
The product may have been exposed to improper temperatures, but the recall does not indicate immediate harm. Proper use of the medication is still safe if it was not affected.
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-0994-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-0994-2022 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.
