American Regent, Inc. Levocarnitine Injection, USP, 1 g/5 mL , 5 mL Single-Dose Vial recall: Labeling: Missing Label
Labeling: Missing Label
The hazard: Drug safety concern
This is an FDA enforcement action. The summary above is the agency’s own description of what went wrong.
What the notice says: Labeling: Missing Label
Why it matters: The FDA recorded an enforcement action against this product. The classification and the summary above describe how serious the agency considers it.
Recall details
- Recall number
- D-0494-2026
- Published
- May 6, 2026
- Risk level
- Class III
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- American Regent, Inc.
- Product type
- Prescription & OTC drugs
- Units affected
- 74,040 Single Dose Vials
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot 24159N0C0, Exp. June 30, 2026 Lot 25193N0C0, Exp. July 31, 2027
Products covered by this recall
Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous use, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC: 0517-1045-01
Check your product
The notice names 12 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Lot or batch code
Usually ink-stamped near the seam, the cap or the bottom of the pack.
- 24159N0C0
- Exp. June 30
- 2026 Lot 25193N0C0
- Exp. July 31
- 2027 — 74
- 04
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- June 30
- 2026 Lot 25193N0C0
- Exp. July 31
NDC number
On the carton and again on the bottle or blister label.
- 0517-1045-01
Package size
Match the net weight or the piece count on the front of the pack.
- 5 mL
- 200 mg
Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Drug safety
American Regent, Inc. — This is an FDA enforcement action. The summary above is the agency’s own description of what went wrong.
- Check the lot number on your pack against the codes listed above.
- Report side effects you think the product caused to FDA MedWatch.
- Do not stop a prescribed medicine on your own — speak to your prescriber or pharmacist first.
- Ask the dispensing pharmacy for a replacement from an unaffected lot.
Refunds and replacements
With medicines, a replacement supply matters more than cash, and that is what pharmacies are set up to provide.
- Ask the dispensing pharmacy for a like-for-like replacement from an unaffected lot. This is the fastest route and usually costs nothing.
- For a mail-order or online pharmacy, use the recall line listed on this page rather than the general support queue.
- If the recall voided a fill you had already paid for, your insurer will normally authorise a replacement ahead of schedule. Quote the recall number.
- If you paid out of pocket, ask for a refund of the co-pay or purchase price and keep the receipt the pharmacy issues.
Company contact: American Regent, Inc. — 6610 New Albany Rd E, New Albany, OH, 43054-8730
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was American Regent, Inc. prescription & otc drugs recalled?
Labeling: Missing Label Labeling: Missing Label
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code 24159N0C0, Exp. June 30, 2026 Lot 25193N0C0; best-by date June 30 or 2026 Lot 25193N0C0. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Check the lot number on your pack against the codes listed above.
Can I get my money back?
Ask the dispensing pharmacy for a like-for-like replacement from an unaffected lot. This is the fastest route and usually costs nothing.
Where was the recalled product sold?
It was distributed nationwide.
Related recalls
-
Class I · last month
American Regent, Inc. Epinephrine Injection, USP, 30 mg/30 mL recall: Presence of Particulate Matter and Lack of Assurance of Sterility
Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and…
-
Class II · 2 months ago
American Regent, Inc. Cyanocobalamin injection USP, 10,000 mcg/10 mL recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
-
Class II · 2 months ago
American Regent, Inc. Multrys , For intravenous infusion recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
-
Class II · 2 months ago
American Regent, Inc. Acetylcysteine Solution, USP, 20% , packaged in a) 4 mL Vial recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
-
Class I · 2 months ago
American Regent, Inc. Papaverine HCl Injection, USP, 60 mg/2 mL recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as glass and/or paraformaldehyde
-
Class II · 2 months ago
American Regent, Inc. Acetylcysteine Solution, USP, 10% , packaged in a) 4 mL Vial recall: Presence of Particulate Matter: Product contaminated with particulate matter
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde