Mckesson Medical-Surgical recalls Aprepitant Capsules (40 mg) due to potential temperature abuse during storage. This may affect prescription products from Sandoz Pharma with NDC 0781-2321-06.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling Aprepitant Capsules (40 mg) because of temperature abuse risks. This could lead to unsafe conditions for patients using the medication.
Temperature abuse during storage can cause the medication to become unsafe. This may happen if the capsules are exposed to temperatures outside the recommended range.
Prescription patients who received Aprepitant Capsules from Mckesson Medical-Surgical. Those with the specific NDC number 0781-2321-06 are most at risk.
Check for the NDC code 0781-2321-06 on the product label. The capsules are prescription-only and come in 40 mg doses from Sandoz Pharma.
Look for the NDC code 0781-2321-06 on the capsule packaging.
The recall indicates potential temperature abuse risks, but the product may still be safe if stored correctly.
Check for the NDC code 0781-2321-06 on the product label. The capsules are prescription-only and from Sandoz Pharma.
The recall does not specify a remedy, so contact your 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-1027-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1027-2022 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.
