OurPharma Fentanyl Injection Solution Short Fill Recall: Underfilled Units

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Recalling firmOurPharma LLC2512 S City Lake Rd, N/A · Fayetteville, AR 72701-5013

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

OurPharma is recalling Fentanyl injection solutions that may be underfilled. This could lead to incorrect dosing during medical procedures, potentially causing harm to patients.

Why it’s dangerous

Underfilled units may not contain the full prescribed dose of Fentanyl. This could result in underdosing during medical procedures, which may not be effective, or overdosing if the concentration is miscalculated.

Who’s affected

Healthcare professionals using the Fentanyl injection solutions for medical purposes. Patients receiving these injections are at risk if the dose is incorrect.

How to tell if you have this one

Check the product label for the NDC number 73013-1001-01. Look for specific lot numbers: 100122080003 (expires 2/26/2023), 100122090001 (expires 3/7/2023), or 100122100002 (expires 4/5/2023).

Brand
OurPharma
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Label
Look for the NDC number 73013-1001-01 on the product label.

✎ GovInfoNow

Questions people ask

What is the hazard with these Fentanyl injections?

The hazard is that the units may be underfilled, which could lead to incorrect dosing during medical procedures.

How can I tell if I have the recalled product?

Check the product label for the NDC number 73013-1001-01 and specific lot numbers: 100122080003 (expires 2/26/2023), 100122090001 (expires 3/7/2023), or 100122100002 (expires 4/5/2023).

What should I do if I have the recalled product?

The recall record does not specify a remedy, so contact OurPharma directly for further instructions.

Take action

Contact OurPharma

We’ve drafted a message you can send OurPharma to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0172-2023 — OurPharma OurPharma

Hello,

I own a OurPharma that is covered by recall D-0172-2023 from OurPharma.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0172-2023 (January 13, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0172-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

OurPharma LLC recalls FentaNYL Citrate 2.5mg/50mL (50mcg/mL) Injection Solution, Preservative-Free IV Injection 50mL Cassette, Rx Only,

Lower-risk recall