Mckesson recalls 500mg amoxicillin capsules due to temperature abuse during storage. This may affect prescription products from Sandoz Pharma with NDC 0781-2613-01. No specific remedy is provided in the recall notice.
cGMP deviations: Temperature abuse
Mckesson is recalling 500mg amoxicillin capsules that may have been exposed to improper temperatures. This could lead to ineffective medication if the capsules were stored incorrectly. The recall affects prescription-only products from Sandoz Pharma with specific NDC numbers.
The recall is for temperature abuse, meaning the capsules may have been stored at temperatures that could affect their stability. This could lead to reduced effectiveness of the medication if the product was not kept at proper storage conditions.
Prescription holders of the 500mg amoxicillin capsules with NDC 0781-2613-01 from Sandoz Pharma are affected. Patients using these capsules for medical treatment are at risk if the product was stored improperly.
Check for the product name 'Amoxicillin Capsules, USP, 500 mg, 100-count bottle' with NDC 0781-2613-01 from Sandoz Pharma. The recall covers prescription-only products distributed by McKesson Medical-Surgical.
Identify the NDC number 0781-2613-01 and confirm it's a prescription-only product from Sandoz Pharma.
The recall is due to potential temperature abuse during storage, which could affect the product's stability and effectiveness.
Look for the product name 'Amoxicillin Capsules, USP, 500 mg, 100-count bottle' with NDC 0781-2613-01 from Sandoz Pharma.
The recall notice does not specify a remedy, so contact your healthcare provider for advice on next steps.
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-1025-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1025-2022 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.
