Mckesson Medical-Surgical recalls 100-count sulfamethoxazole and trimethoprim tablets (800mg/160mg) due to temperature abuse risks. The recall affects prescription products from Major Pharma with NDC 0904-2725-61.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical is recalling prescription sulfamethoxazole and trimethoprim tablets (800mg/160mg) because of temperature abuse risks. This could lead to improper drug stability and potential safety issues for patients.
The recall is due to cGMP deviations related to temperature abuse. This means the medication may have been exposed to temperatures that compromise its stability, potentially affecting its effectiveness or safety.
Prescription patients who received the specific product from Major Pharma with NDC 0904-2725-61. Healthcare providers and pharmacies handling these products may also be affected.
Check for the product name 'Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg' in a 100-count unit dose box. The manufacturer is Major Pharma with NDC 0904-2725-61. This product is prescription-only.
Verify the product name, strength, and NDC number to confirm if it matches the recalled items.
The recall is due to cGMP deviations related to temperature abuse, which could affect the medication's stability.
Check for the product name 'Sulfamethoxazole and Trimethoprim Tablets, USP, 800mg/160mg' in a 100-count unit dose box with NDC 0904-2725-61.
The recall does not 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-1059-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1059-2022 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.
