Natures Pharmacy recalls hydroxyprogesterone caproate due to potential sterility issues from quality control failures observed during FDA inspection. All lots within expiry are affected.
Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.
Natures Pharmacy & Comp: Hydroxyprogesterone caproate is being recalled because of potential sterility risks from quality control failures during an FDA inspection. This could affect patients using the medication.
The medication may not be sterile due to quality control issues observed during an FDA inspection. This could lead to infections or other health risks for patients using the product.
Patients using hydroxyprogesterone caproate from Natures Pharmacy & Compounding Center are affected. Those with medical conditions requiring this medication are at higher risk.
Check the lot number on your hydroxyprogesterone caproate bottle. All lots within expiry are affected by this recall.
Identify the lot number on your hydroxyprogesterone caproate bottle to confirm if it is affected.
The recall indicates potential sterility risks, so it is not safe to use without checking the lot number and following the recall instructions.
The official recall record does not specify how to obtain the recalled product.
The official recall record does not specify what to do with the recalled product.
We’ve drafted a message you can send Natures Pharmacy & Compounding Center to request your refund or repair — edit it as you like.
Subject: Recall D-1121-2014 — Natures Pharmacy & Compounding Center Natures Pharmacy & Compounding Center Hello, I own a Natures Pharmacy & Compounding Center that is covered by recall D-1121-2014 from Natures Pharmacy & Compounding Center. 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.
