FDA Drug Recalls

Recalls / Class II

Class IID-0295-2025

Product

fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine HCl 100 mg/100 mL (1 mg/mL), 100 ml in NS Yellow CADD FSFF, Injection for Epidural Use (Not intended For IV Use), Compounded, For Institutional or Office Use Only, QuVa Pharma, 1075 West Park One Drive, Suite 100, Sugar Land, Tx 77478. NDC: 70092-1255-75

Affected lot / code info
Lots: 10140259, 10140539, 10140687, 10140688; Exp 04/24/2025

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
QuVa Pharma, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
1075 W Park One Dr Ste 100, N/A, Sugar Land, Texas 77478-2576

Distribution

Quantity
N/A
Distribution pattern
U.S. Nationwide

Timeline

Recall initiated
2025-03-06
FDA classified
2025-03-25
Posted by FDA
2025-04-02
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-0295-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.