Pharmacy Plus Inc. recalls sterile medroxyprogesterone acetate 300mg/ml suspension vials after FDA found production couldn't guarantee sterility. Do not use these products.
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Pharmacy Plus Inc. is recalling medroxyprogesterone acetate 300 mg/ml suspension vials because they were produced without proper sterility assurance. This could lead to infections if used improperly.
FDA inspections found the products were made without sufficient sterility assurance. This means the medication might not be sterile, increasing the risk of infections when injected.
People with prescriptions for this medication from pharmacies that sold the recalled vials. Those using the product without proper sterility could face infections.
Check for vials labeled 'MEDROXYPROGESTERONE ACETATE 300 MG/ML Suspension, 10 mL vial, Rx only' from Vital Care Compounder. The lot number 55786 with a batch date ending December 31, 2022.
Do not use the recalled medroxyprogesterone acetate suspension vials as they may cause infections.
FDA inspections found the products were produced without sufficient sterility assurance, which could lead to infections if used.
Look for vials labeled 'MEDROXYPROGESTERONE ACETATE 300 MG/ML Suspension, 10 mL vial, Rx only' with lot number 55786 and batch date ending December 31, 2022.
Stop using the product immediately as it may cause infections.
We’ve drafted a message you can send Vital Care Compounder to request your refund or repair — edit it as you like.
Subject: Recall D-0037-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0037-2023 from Vital Care Compounder. 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.
