New Life Pharma recalls 2mg Semaglutide injections due to potential lack of sterility. This could cause infections if used. Affected units have specific lot and expiration details.
Lack of Assurance of Sterility
New Life Pharma is recalling 2mg Semaglutide injections that may not be sterile, which could lead to infections. This recall affects patients using the medication as prescribed.
The vials may not be sterile, meaning they could contain harmful bacteria. If injected, this could cause serious infections or other health issues. The risk is not yet confirmed but is a potential hazard.
Patients prescribed Semaglutide injections by a doctor are affected. Those using the recalled vials for weight management or diabetes treatment are at risk.
Check for the product name 'Semaglutide Inj., 2 mg x 5, Sterile Multi-Dose Vial' with NDC 84223-001-06. The lot number is 240903 and expiration date is 9/30/2026.
Look for the NDC code 84223-001-06 and lot number 240903 on the vial label.
The recall states there is a potential lack of sterility, but no specific safety confirmation is provided in the record.
The recall record does not specify a remedy, so no action is required beyond checking the product details.
Check the NDC code 84223-001-06 and lot number 240903 on the vial label.
We’ve drafted a message you can send New Life Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0393-2026 — New Life Pharma New Life Pharma Hello, I own a New Life Pharma that is covered by recall D-0393-2026 from New Life Pharma. 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.
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