APS Pharmacy recalls testosterone cypionate/anastrozole oil injectable products with lack of sterility assurance. Affected lots include 745383, 759295, 745749, and 746272. Consumers should contact APS Pharmacy for details.
Lack of sterility assurance.
APS Pharmacy is recalling testosterone cypionate/anastrozole oil injectable products due to a lack of sterility assurance. This could lead to infections if the product is used. The recall affects specific lots manufactured between June 2022 and August 2022.
The product lacks sterility assurance, meaning it may not be free from harmful bacteria or contaminants. If used, this could lead to infections or other health issues. The exact risk level depends on the specific lot and usage conditions.
Individuals who have received testosterone cypionate/anastrozole oil injectable products from APS Pharmacy in the specified lots are affected. Patients using these products for hormone therapy are most at risk.
Check the product label for the lot numbers: 745383, 759295, 745749, or 746272. These lots were manufactured between June and August 2022 by APS Pharmacy.
Look for the lot numbers on the vial: 745383, 759295, 745749, or 746272.
APS Pharmacy is recalling testosterone cypionate/anastrozole oil injectable products with specific lot numbers: 745383, 759295, 745749, and 746272.
The product lacks sterility assurance, which could lead to infections if used.
Check the product label for the lot numbers: 745383, 759295, 745749, or 746272.
We’ve drafted a message you can send APS Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0730-2022 — APS Pharmacy APS Pharmacy Hello, I own a APS Pharmacy that is covered by recall D-0730-2022 from APS Pharmacy. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
