Olympia Pharmacy recalls NAD+ Nicotinamide Adenine Dinucleotide powder for reconstitution with potential sterility issues. This Rx-only product may pose infection risks if not properly sterilized.
Lack of assurance of sterility.
Olympia Pharmacy is recalling NAD+ Nicotinamide Adenine Dinucleotide powder for reconstitution due to lack of sterility assurance. This could lead to infections if the product is not properly sterilized before use.
The product lacks proper sterility assurance, meaning it could contain harmful bacteria or other contaminants. If not properly sterilized before use, this could lead to infections in patients.
Prescription patients who received the recalled NAD+ powder for reconstitution. Those with compromised immune systems may be at higher risk of infection.
Check for the product name 'NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial'. Look for lots A2401422, BUD 1/14/2023; K41001, BUD 11/1/2022; K41130, BUD 11/30/2022; L24113, BUD 12/13/2022; or L41102, BUD 12/2/2022.
Verify the product name and lot numbers listed in the recall notice to confirm if your product is affected.
The product lacks sterility assurance, so it may contain harmful contaminants. Do not use until the recall remedy is followed.
Check for the product name 'NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial' and lot numbers A2401422, K41001, K41130, L24113, or L41102.
The recall remedy is not specified in the notice, so contact Olympia Pharmacy directly for guidance.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0939-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0939-2022 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.
