Sun Pharmaceutical recalls certain medroxyprogesterone acetate injectable suspensions (1mL, 150mg/mL) due to lack of sterility assurance. This could lead to infections if used improperly. Affected lots and expiration dates listed.
Lack of assurance of sterility
Sun Pharmaceutical is recalling specific medroxyprogesterone acetate injectable suspensions because they may not be sterile. Using these products could lead to infections, especially in medical settings where sterility is critical.
The injectable suspension may not be sterile, which could cause infections if used improperly. This is a risk in medical settings where sterility is critical for patient safety.
Healthcare providers and patients prescribed this medication by a doctor. Those using the recalled products for medical treatment are most at risk.
Check for the product name: medroxyprogesterone acetate injectable suspension (1mL, 150mg/mL). Look for lot numbers JKX4312A, JKX4313A (exp 09/2022), JKX4827A (exp 09/2023), HAC1290A, HAC2082B (exp 06/2023).
Look for lot numbers JKX4312A, JKX4313A (exp 09/2022), JKX4827A (exp 09/2023), HAC1290A, HAC2082B (exp 06/2023) on the product label.
The product may not be sterile, which could lead to infections. Do not use these specific lots without consulting a healthcare provider.
Check the lot number on the product label. If it matches the recalled lots, contact your healthcare provider for guidance.
The recall record does not specify a replacement process. Contact your healthcare provider for assistance.
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-1143-2022 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-1143-2022 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.
