CLASS II ONGOING Drug recall · Reported 26 Aug 2026 · FDA Enforcement Report

Nitroglycerin injection, USP, 50 mg/ (5 mg/mL) recalled

American Regent is recalling Nitroglycerin injection, USP, 50 mg/ (5 mg/mL), distributed nationwide in the US. The recall was initiated on 24 Jul 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 24291, Exp. Date: 8/31/2026
NDC0517-4810
UPC0305174810258
Quantity recalled98,200 vials

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0791-2026
FDA event ID
99503
Recalling firm
American Regent, Shirley, NY
Manufacturer
American Regent, Inc.
Classification
Class II
Status
Ongoing
Recall initiated
24 Jul 2026
FDA classified
26 Aug 2026
Reported
26 Aug 2026
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Particulate Matter

Timeline

24 Jul 2026Recall initiated by company
26 Aug 2026Classified by FDA+33 days
26 Aug 2026Published in enforcement report+0 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

Product as listed by the FDA

Nitroglycerin injection, USP, 50 mg/10 mL (5 mg/mL), packaged in a) 10 mL vials (NDC 0517-4810-01), b) 25x10mL vials (NDC 0517-4810-25) RX only, AMERICAN REGENT, INC., Shirley, NY 11967.

Where it was distributed

Nationwide within the U.S

Nationwide

Questions about this recall

Is Nitroglycerin injection, USP, 50 mg/ (5 mg/mL) recalled?

Yes. American Regent recalled Nitroglycerin injection, USP, 50 mg/ (5 mg/mL) on 24 Jul 2026. The recall is Class II and its status is Ongoing. Recall number D-0791-2026.

Why was it recalled?

Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde

Which lots are affected?

Lot #: 24291, Exp. Date: 8/31/2026

Where was it sold?

Nationwide within the U.S

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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