NAD+ Injection Recall: Apothecary 200 mg/mL vial
Announced 2026-10-14 · FDA
Apothecary NAD+ Injection 200 mg/mL, 6 mL sterile multi-dose vial, Rx Only, is being recalled nationwide due to lack of assurance of sterility. The recall involves lot AP-202647 with a BUD of 13-Oct-2026.
| Brand | Apothecary Pharma LLC |
|---|---|
| Product | Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vial, Rx Only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC, 27513, NDC 85091-011-06. |
| Reason | Lack of Assurance of Sterility |
| Severity | moderate |
| Units affected | 22 |
| Distribution | Nationwide within the United States |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use the recalled NAD+ Injection if you have it.
- Check your vials for lot AP-202647 and confirm the BUD date of 13-Oct-2026; set affected product aside.
- Contact your healthcare provider or the recalling entity for guidance on return, disposal, or replacement.
How to identify the recalled item
| Lot / date codes | Lot #: AP-202647, BUD 13-Oct-2026 |
|---|---|
| Lot / date codes | Lot #: AP-202622, BUD 07-Oct-2026; AP-202623, BUD 08-Oct-2026; AP-202624, BUD 19-Oct-2026; AP-202625, BUD 10/20/2026; AP-202627, BUD 10/26/2026; AP-202628, BUD 10/27/2026; AP-202629, BUD 10/28/2026; AP-202630, BUD 10/31/2026; AP-202631, BUD 11/01/2026; AP-202632, BUD 11/03/2026; AP-202633, BUD 11/07/2026; AP-202634, BUD 11/08/2026; AP-202635, BUD 11/16/2026; AP-202636, BUD 11/17/2026; AP-202637,BUD 11/18/2026; AP-202638, BUD 11/19/2026; AP-202639, BUD 11/20/2026; AP-202640, BUD 11/21/2026;AP-202641, BUD 11/22/2026; AP-202642, BUD 11/24/2026; AP-202643, BUD 11/25/2026; AP-202644, BUD 11/26/2026 |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.