Class I · High risk Ongoing
Nad+
Reason Microbial Contamination of Sterile Products: elevated endotoxin levels
NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder for reconstitution
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated
What was recalled
NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder for reconstitution, Multi-Dose 500 mg Per Vial, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0083-00
- Recalling firm
- Olympia Compounding Pharmacy dba Olympia Pharmacy
- NDC code
- 73198-0083-00
- Origin
- FL, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0795-2022
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Nicotinamide recalls
See all
Class II · Moderate risk Ongoing
Nad+
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Nicotinamide adenine dinucleotide
Reason Lack of Assurance of Sterility
Class II · Moderate risk Ongoing
Nicotinamide adenine dinucleotide
Reason Lack of Assurance of Sterility
Class II · Moderate risk Completed
NAD+ Nicotinamide Adenine Dinucleotide
Reason Lack of assurance of sterility.
Get an alert if your medication is recalled
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.