IPAMORELIN 2000MCG/ML INJ in 2 mL vial Assurance Infusion (713) 533-8800

FDA Recall #D-0748-2020 — Class II — December 20, 2019

Recall #D-0748-2020 Date: December 20, 2019 Classification: Class II Status: Terminated

Product Description

IPAMORELIN 2000MCG/ML INJ in 2 mL vial Assurance Infusion (713) 533-8800

Reason for Recall

Lack of sterility assurance.

Recalling Firm

Assurance Infusion — Houston, TX

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

5 vials

Distribution

Nationwide within the United States

Code Information

Lots: 07162019@20 Exp. 01/12/2020; 12102019@17 Exp. 06/07/2020; 07162019@20 Exp. 01/12/2020

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated