OurPharma LLC: Drug Recall
Recall #D-0385-2025 · 04/15/2025
Class III: Low Risk
Recall Details
- Recall Number
- D-0385-2025
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- OurPharma LLC
- Status
- Ongoing
- Date Initiated
- 04/15/2025
- Location
- Fayetteville, AR, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,375 cassettes
Reason for Recall
Superpotent Drug: Assay/potency result for hydromorphone HCl in the compounded stability lot was higher than specification..
Product Description
HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL), packaged in a 50 mL Cassette, Rx Only, OurPharma, LLC, 2512 S. City Lake Rd., Fayetteville, AR 72701, NDC 73013-1040-01.
Distribution Pattern
Nationwide in the USA
Other Recalls by OurPharma LLC
- Class III: Low Risk 01/13/2023
- Class II: Risk 11/29/2022
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.