PlainRecalls
FDA Drug Moderate Class II Terminated

Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31

Reported: March 27, 2019 Initiated: February 15, 2019 #D-1065-2019

Product Description

Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31

Reason for Recall

Subpotent Drug.

Details

Units Affected
11888 units
Distribution
Nationwide within the United States
Location
East Brunswick, NJ

Frequently Asked Questions

What product was recalled?
Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31. Recalled by Heritage Pharmaceuticals, Inc.. Units affected: 11888 units.
Why was this product recalled?
Subpotent Drug.
Which agency issued this recall?
This recall was issued by the FDA Drug on March 27, 2019. Severity: Moderate. Recall number: D-1065-2019.