Quva Pharma, Inc.: Methohexital Sodium, 100 Mg/10 Ml (10 Mg/ml), Total Volume

Recall Summary QuVa Pharma is recalling Methohexital Sodium 100 mg/10 mL vials (a prescription anesthetic drug) distributed nationwide because the product failed quality tests for impurities and degradation. This is a Class II recall, meaning the product could cause serious health problems or death. The affected vials have product code 70092-1310-46 and were distributed across all U.S. states and Washington D.C.

Recalling firm

QuVa Pharma, Inc.

Product

Methohexital Sodium, 100 mg/10 mL (10 mg/mL), Total Volume: 10 mL, Rx only, Compounded drug, QuVa Pharma, 1075 W Park One Dr, Suite 100, Sugar Land, TX 77478, Product code: 70092-1310-46.

Reason

Failed Impurities/Degradation Specifications

Classification

Class II

Category

drug recall

Country

United States

Agency

U.S. Food and Drug Administration

Recall date

2026-06-24

Status

Ongoing

Areas affected

AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...

Distribution

Nationwide within the United States

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/3ef94e41-8fd8-4bc3-9232-c06b2fb4a5d3