MORPHINE 20MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

FDA Recall #D-0755-2020 — Class II — December 20, 2019

Recall #D-0755-2020 Date: December 20, 2019 Classification: Class II Status: Terminated

Product Description

MORPHINE 20MG/ML INJ in 20 mL syringe 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

3 syringes

Distribution

Nationwide within the United States

Code Information

Lot: 12102019@7 Exp. 12/19/2019; 12112019@11 Exp. 12/20/2019; 12162019@5 Exp. 12/25/2019

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated