FDA Drug Recalls

Recalls / Class II

Class IID-0565-2020

Product

fentaNYL 200 mcg/100 mL (2 mcg/mL) BUPivacaine HCl 0.1% 100 mg/100 mL (1 mg/mL) in 0.9% Sodium Chloride Preservative Free 100 mL in 150 mL Bag, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1103-36

Affected lot / code info
Lots: 10029200 Exp. 11/18/2019, 10030347 Exp. 11/24/2019, 10031325 Exp. 12/16/2019, 10030939 Exp. 12/3/2019, 10031865 Exp. 12/24/2019, 10031758 Exp. 12/26/2019, 10031757 Exp. 12/26/2019, 10032275 Exp. 12/30/2019

Why it was recalled

Presence of Particulate matter: manufacturer recalled fentanyl API due to potential for glass particules

Recalling firm

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

Distribution

Distribution pattern
Nationwide.

Timeline

Recall initiated
2019-11-12
FDA classified
2019-12-03
Posted by FDA
2019-12-11
Terminated
2020-06-05
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0565-2020. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.