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Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vial, Rx Only Recall 2026

Apothecary Pharma LLCIssued September 24, 2026Updated Reviewed by the Recall Watch editorial team

Apothecary Pharma LLC 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. — recalled per FDA on 9/24/2026. Reason: Lack of Assurance of Sterility.

Agency
FDA
Issued
Sep 24, 2026
Brand
Apothecary Pharma LLC
Distribution
1 states
Lots affected
2
What to do right now

Steps to take for this recall

  1. Stop using it

    Take it out of rotation. Don't consume, wear, or operate.

  2. Verify the match

    Compare lot numbers, UPCs, and dates against your product.

  3. Return or dispose

    Follow the manufacturer's instructions to refund or safely dispose.

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Verified summary of the official U.S. Food and Drug Administration notice · Issued September 24, 2026 · Last synced Oct 21, 2026

What's recalled

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.

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Why it was recalled

Lack of Assurance of Sterility

Affected products & lot numbers
2 lots called out

Affected Lot Numbers

Check your product label — do not use if your lot number appears below.

Lot Number
Lot #: AP-202647
BUD 13-Oct-2026
Where was it sold
1 state

Nationwide within the United States

nationwide
Official noticefda.gov
More recalls like this
5 related — by brand, contaminant, and category

Frequently asked questions

Is the Apothecary Pharma LLC recall still active?

Yes, this recall is currently active as of September 24, 2026. Do not use or consume the affected product.

What lot numbers are affected?

Affected lot numbers: Lot #: AP-202647, BUD 13-Oct-2026. Check the label on your product.

What should I do if I have the recalled Apothecary Pharma LLC?

Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.