FDA recall D-0377-2021

Teva Pharmaceuticals USA · Class II · drug

Product

Metoclopramide Injection USP, 10 mg/2 mL (5 mg/mL), 2 mL Single-Use Vial, Rx Only, TEVA Parenteral Medicines, Inc. Irvine, CA 92618 NDC 0703-4502-04

Reason for recall

Lack of Assurance of Sterility

Distribution

Product was distributed nationwide.

Key facts

Status
Terminated
Initiation date
2021-04-26
Report date
2021-05-26
Termination date
2024-06-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Parsippany, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0377-2021