Olympia Pharmacy recalls NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder due to failed reconstitution. This may affect prescription medication safety. Check product details to determine if your item is affected.
Failed Reconstitution time
Olympia Pharmacy is recalling NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder for reconstitution because it may fail to reconstitute properly. This could lead to unsafe medication concentrations if used incorrectly.
The powder may not reconstitute correctly when mixed with water, leading to improper medication concentration. This could cause unsafe drug levels if the product is used as intended.
Prescription drug users who have the specific NAD+ powder with NDC 73198-0083-00 and lot number F41116. Patients using this medication for medical purposes are most at risk.
Check for the product name 'NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder', NDC 73198-0083-00, and lot number F41116. This medication is sold by Olympia Pharmacy in Orlando, Florida.
Identify the NDC code 73198-0083-00 and lot number F41116 to confirm if your product is affected.
The recall states there is a risk of failed reconstitution, but the official notice does not specify if the product is safe to use after reconstitution.
Check for the NDC code 73198-0083-00 and lot number F41116 on the product label.
The recall record does not specify a remedy, so the official notice does not state what action to take.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0828-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0828-2022 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.
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.