APS Pharmacy recalls Gonadorelin (5ml) 0.2 mg/ml injectable vials with specific batch numbers due to lack of sterility assurance. This could pose infection risks if used.
Lack of sterility assurance.
APS Pharmacy is recalling Gonadorelin injectables that may not be sterile, which could lead to infections if used. This affects patients receiving hormone therapy.
The injectable vials lack sterility assurance, meaning they could be contaminated with bacteria. If injected, this could cause infections, though the risk is low for most users.
Patients using Gonadorelin for hormone therapy are affected. Those with compromised immune systems may be at higher risk.
Check the vial label for the product name 'GONADORELIN (5ML) 0.2 MG/ML INJECTABLE' and batch numbers listed in the recall (e.g., 745708, 753364).
Look for the product name and batch numbers listed in the recall notice to confirm if your vial is affected.
The recall states there is a lack of sterility assurance, so affected vials may not be safe. Do not use until confirmed safe.
Check the vial label for batch numbers listed in the recall. If it matches, stop using it and contact APS Pharmacy for instructions.
The recall record does not specify a replacement process. Contact APS Pharmacy directly for assistance.
We’ve drafted a message you can send APS Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0728-2022 — APS Pharmacy APS Pharmacy Hello, I own a APS Pharmacy that is covered by recall D-0728-2022 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.
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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.
