Teva Pharmaceuticals USA recalls 10mL multiple-dose vials of Methylprednisolone Acetate Injectable Suspension due to lack of sterility assurance. This could lead to infections if used improperly.
Lack of Assurance of Sterility
Teva Pharmaceuticals USA is recalling a specific injectable steroid medication because it may not be sterile. Using this product could lead to infections, especially in medical settings where sterility is critical.
The product lacks assurance of sterility, meaning it might contain harmful bacteria or other contaminants. This could cause infections if the medication is injected into the body, particularly in medical settings where sterility is critical.
Patients prescribed this medication by a doctor are affected. Healthcare providers using the product for injections may be at higher risk due to the potential for infection.
Check for the product name 'Methylprednisolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL)', 10 mL Multiple-Dose Vial, Rx Only. Look for lot number 100022393 with expiration date 09/2022.
Identify the product by checking the label for the specific name, lot number 100022393, and expiration date of 09/2022.
The recall states there is a lack of assurance of sterility, so it may not be safe to use. The product should not be used until a replacement is obtained.
Check the product label for the name 'Methylprednisolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL)', 10 mL Multiple-Dose Vial, Rx Only, lot number 100022393, and expiration date 09/2022.
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe alternatives.
We’ve drafted a message you can send Teva Pharmaceuticals USA to request your refund or repair — edit it as you like.
Subject: Recall D-0370-2022 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA Hello, I own a Teva Pharmaceuticals USA that is covered by recall D-0370-2022 from Teva Pharmaceuticals USA. 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.
