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D-0828-2022 Class II Terminated

Recalled by Olympia Compounding Pharmacy Dba Olympia Pharmacy — Orlando, FL

FDA drug recall D-0828-2022 was initiated by Olympia Compounding Pharmacy Dba Olympia Pharmacy on Apr 4, 2022 and is designated Class II. Reason for recall: Failed Reconstitution time The recall status is terminated (terminated Jun 17, 2024).

Recall Details

Product Type: Drugs
Report Date: May 4, 2022
Initiation Date: Apr 4, 2022
Termination Date: Jun 17, 2024
Voluntary/Mandated: Voluntary: Firm initiated

Product Description

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

Reason for Recall

Failed Reconstitution time

Distribution Pattern

Distributed Nationwide in the USA

Code Information

Lot: F41116 BUD: 6/16/2022,

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0828-2022
openFDA file date: Oct 23, 2026
Loaded by RegDataLab: Oct 26, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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