Sun Pharmaceutical recalls 150 mg/mL medroxyprogesterone acetate injectables with sterility concerns. This product may cause infections if not properly sterilized.
Lack of assurance of sterility
Sun Pharmaceutical is recalling a specific injectable medication due to a lack of sterility assurance. This could lead to infections if the product is used without proper sterilization.
The product lacks assurance of sterility, meaning it may not be clean enough to prevent infections when injected. This risk is specific to medical use and not a general safety hazard.
Patients prescribed this medication by a doctor. Those using the product without medical supervision are at higher risk.
Check for the product name 'medroxyprogesterone acetate injectable suspension, USP, 1 mL prefilled syringe, 150 mg/mL'. It was manufactured by Sun Pharmaceutical Industries Ltd. in India and distributed by Sun Pharmaceutical Industries, Inc. in the US.
Look for the NDC code 62756-091-40 and lot number HAC1951A on the syringe label.
The product has a lack of sterility assurance, which could lead to infections if used improperly. Do not use without medical supervision.
Check for the NDC code 62756-091-40 and lot number HAC1951A on the syringe label.
Contact your doctor or pharmacist for guidance on whether to stop using the product.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-1145-2022 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-1145-2022 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.
