Sun Pharmaceutical recalls certain medroxyprogesterone acetate injectable vials (150 mg/mL) due to lack of sterility assurance. This may pose a risk of infection. Affected lots and expiration dates are listed in the recall notice.
Lack of assurance of sterility
Sun Pharmaceutical is recalling specific lots of medroxyprogesterone acetate injectable suspension vials because they lack sterility assurance. This could lead to infections if used improperly. Patients with a prescription for this medication should check their lot numbers and expiration dates.
The product lacks proper sterility assurance, which means it could contain harmful bacteria or other contaminants. This poses a risk of infection when injected into the body, especially in medical settings where sterility is critical.
Patients prescribed medroxyprogesterone acetate injections by a healthcare provider. Those using the recalled lots are at risk of infection if the product is not sterile.
Check the vial label for the lot number and expiration date. The recalled lots include HAC2075A (exp 06/2023), HAC2076A (exp 07/2023), and others listed in the recall notice.
Look for the lot number and expiration date on the vial label to determine if it is recalled.
The product lacks sterility assurance, which could lead to infections. Do not use the recalled lots.
Check the vial label for the lot number and expiration date. If it matches the recalled lots listed in the notice, stop using it and contact your healthcare provider.
Check the vial label for the lot number and expiration date. Compare it to the list of recalled lots provided in the recall notice.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-1146-2022 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-1146-2022 from Sun Pharmaceutical. 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.
