Olympia Pharmacy recalls Sermorelin Acetate Lyophilized powder for reconstitution (9mg/vial) due to potential sub-potent levels. This may affect growth hormone treatment efficacy. Check NDC 73198-0059-00 for affected products.
Sub Potent
Olympia Pharmacy is recalling Sermorelin Acetate Lyophilized powder for reconstitution (9mg/vial) because it may be sub-potent. This could mean the product doesn't work as intended for growth hormone treatment. Affected patients should contact their doctor to discuss alternatives.
The product may contain lower-than-stated active ingredient levels, potentially reducing treatment effectiveness. This could lead to inadequate hormone levels in patients who rely on the medication for growth or other medical conditions.
Patients using Sermorelin Acetate Lyophilized powder for growth hormone treatment. Those with specific medical conditions requiring precise hormone levels may be most affected.
Check for the NDC code 73198-0059-00 on the product label. Products were sold with lots D44026 (expiring 4/26/22) and F42104 (expiring 6/4/22).
Discuss alternative treatment options with your healthcare provider as the product may not work as intended.
The product may be sub-potent, meaning it could have lower-than-stated active ingredient levels. This might reduce treatment effectiveness but does not cause immediate harm.
Contact your doctor to discuss alternative treatment options. The product does not need to be discarded as it is not unsafe but may not work as intended.
Look for the NDC code 73198-0059-00 on the product label. Products were sold with lots D44026 (expiring 4/26/22) and F42104 (expiring 6/4/22).
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0718-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0718-2022 from Olympia 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.
