STAQ Pharma, Inc. FentaNYL Citrate PF, 500mcg/50 mL in Nacl, Injection for IV use recall: Labeling: Incorrect or Missing Lot and/or Exp Date
Labeling: Incorrect or Missing Lot and/or Exp Date
The hazard: Drug safety concern
A problem with this medicine prompted the recall. With prescriptions, the first move is a conversation rather than a decision.
What the notice says: Labeling: Incorrect or Missing Lot and/or Exp Date
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-0025-2026
- Published
- October 22, 2025
- Risk level
- Class III
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- STAQ Pharma, Inc.
- Product type
- Prescription & OTC drugs
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot: 25102464B, Expiry: 26NOV2025; 25102370A, Expiry: 20OCT2025; 25102369A, Expiry: 19OCT2025.
Products covered by this recall
FentaNYL Citrate PF, 500mcg/50 mL (10mcg/mL) in NACL, Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0102-05.
Check your product
The notice names 6 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.
- 25102464B
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- 26NOV2025
- 20OCT2025
- 19OCT2025
NDC number
On the carton and again on the bottle or blister label.
- 73177-0102-05
Package size
Match the net weight or the piece count on the front of the pack.
- 50 mL
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
STAQ Pharma, Inc. — A problem with this medicine prompted the recall. With prescriptions, the first move is a conversation rather than a decision.
- 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.
Getting a replacement supply
Do not let a refund question interrupt your treatment. Deal with the supply first and the money second.
- Call the pharmacy before you run low. They can see which lot they dispensed to you and will usually swap it the same day.
- Insurers do not normally count a recall replacement against a refill limit. If one is refused, ask the pharmacist to call it through as a recall override.
- Over-the-counter products are refunded at the till like any other purchase; the recall notice on your phone is enough to explain the return.
- If the manufacturer runs a direct reimbursement form, it will be linked from the official notice on this page.
Company contact: STAQ Pharma, Inc. — 14135 E 42nd Ave Ste 50, Denver, CO, 80239-5214
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 STAQ Pharma, Inc. prescription & otc drugs recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date Labeling: Incorrect or Missing Lot and/or Exp Date
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code 25102464B; best-by date 26NOV2025 or 20OCT2025. 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?
Call the pharmacy before you run low. They can see which lot they dispensed to you and will usually swap it the same day.
Where was the recalled product sold?
It was distributed nationwide.
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