Fresh Recalls

Apothecary NAD+ Injection 200 mg/mL: recall status

Notice names this product. Apothecary Pharma’s Apothecary NAD+ Injection 200 mg/mL is named in FDA Class II recall D-0037-2027. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: Lack of Assurance of Sterility Identifying details: Lot #: AP-202647, BUD 13-Oct-2026. Units affected: 1 vial. Status: Ongoing.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Apothecary NAD+ Injection 200 mg/mL
Company / brand
Apothecary Pharma
Lot / serial / date codes
Lot #: AP-202647, BUD 13-Oct-2026
Distribution
Nationwide within the United States
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

Brand
Apothecary Pharma

Recalls naming this model

FDA Class II · Drug · October 14, 2026

Apothecary NAD+ Injection 200 mg/mL recall — Apothecary Pharma LLC

Lack of Assurance of Sterility

Company / brand: Apothecary Pharma recalls

Affected product: Apothecary NAD+ Injection 200 mg/mL recall status

Official ID D-0037-2027 · Official record ↗

See all Apothecary Pharma recalls →

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 12:00 PM UTC.