Teva Pharmaceuticals recalls specific lots of Methylprednisolone Acetate Injectable Suspension due to lack of sterility assurance. This medication may cause infection if used.
Lack of Assurance of Sterility
Teva Pharmaceuticals is recalling certain lots of Methylprednisolone Acetate Injectable Suspension because the product may not be sterile. This could lead to serious infections if the medication is used.
The medication may not be sterile, which means it could cause infections if injected. This is a serious risk for patients who need this medication for medical conditions.
People who have been prescribed this medication by a doctor and received the recalled lots are affected. Those using the medication for medical treatment are at risk of infection.
Check the product label for the lot numbers listed: 31328455B, 31329340B, 31329439B, 31328347B, 31328321B, 31328368B, 31328394B, 31328699B, 31328834B, and 31329286B. The product is available in 1 mL single-dose vials and 5mL/10mL multi-dose vials.
Look for the lot numbers listed in the recall notice to determine if your medication is affected.
The recall notice states that the medication may not be sterile, which could lead to infections. Do not use the affected lots.
Check the product label for the lot numbers listed in the recall notice. If you have the affected lots, do not use them and contact your healthcare provider.
Check the product label for the lot numbers: 31328455B, 31329340B, 31329439B, 31328347B, 31328321B, 31328368B, 31328394B, 31328699B, 31328834B, and 31329286B.
We’ve drafted a message you can send Teva Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0731-2021 — Teva Pharmaceuticals Teva Pharmaceuticals Hello, I own a Teva Pharmaceuticals that is covered by recall D-0731-2021 from Teva Pharmaceuticals. 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.
