Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Low RiskFDA Drug
Medications & Supplements/Prescription Drugs

OurPharma Fentanyl Citrate Injection Cassettes Recalled for Underfilling

Agency Publication Date: January 23, 2023
Share:
Sign in to monitor this recall

Summary

OurPharma LLC has recalled 768 cassettes of Fentanyl Citrate 2.5mg/50mL (50mcg/mL) Injection Solution. The recall was issued because these cassettes were found to be underfilled, which means they do not contain the full amount of medication. No injuries or incidents have been reported to date.

Risk

Underfilled cassettes may lead to a patient receiving a lower dose of pain medication than prescribed, potentially resulting in inadequate pain management during medical procedures.

What You Should Do

  1. This recall affects Fentanyl Citrate 2.5mg/50mL (50mcg/mL) Injection Solution, Preservative-Free IV Injection 50mL Cassettes sold under the OurPharma, LLC brand (NDC 73013-1001-01). Affected lot numbers are 100122080003 (Exp. 2/26/2023), 100122090001 (Exp. 3/07/2023), and 100122100002 (Exp. 4/05/2023).
  2. Stop using the recalled product immediately. Contact the manufacturer or your medical distributor to arrange for the return of any remaining units.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Fentanyl Citrate 2.5mg/50mL (50mcg/mL) Injection Solution
Variants: Preservative-Free, IV Injection, 50mL Cassette, Rx Only
Lot Numbers:
100122080003 (Exp. 2/26/2023)
100122090001 (Exp. 3/07/2023)
100122100002 (Exp. 4/05/2023)
NDC:
73013-1001-01

Recall #: D-0172-2023; Distributed by OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91520
Status: Resolved
Manufacturer: OurPharma LLC
Sold By: Rx Only; Hospitals; Healthcare Facilities
Manufactured In: United States
Units Affected: 768 cassettes
Distributed To: Illinois, Missouri

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.