Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

NAD+ Nicotinamide Adenine Dinucleotide Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due to Product found to be Sub Potent or Exceeded...

Date: March 8, 2022
Company: Olympia Compounding Pharmacy dba Olympia Pharmacy
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Olympia Compounding Pharmacy dba Olympia Pharmacy directly.

Affected Products

NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial, Each ML contains: 0.288% Sodium Phosphate Monobasic USP, 0.42% Sodium Phosphate Dibasic USP, 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835 NDC: 73198-0083-00

Quantity: 2634 vials

Why Was This Recalled?

Product found to be Sub Potent or Exceeded reconstitution time

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Olympia Compounding Pharmacy dba Olympia Pharmacy

Olympia Compounding Pharmacy dba Olympia Pharmacy has 94 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report