PlainRecalls
FDA Drug Moderate Class II Terminated

FENTANYL 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Reported: January 22, 2020 Initiated: December 20, 2019 #D-0732-2020

Product Description

FENTANYL 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Reason for Recall

Lack of sterility assurance.

Details

Recalling Firm
Assurance Infusion
Units Affected
1 syringe
Distribution
Nationwide within the United States
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
FENTANYL 5MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800. Recalled by Assurance Infusion. Units affected: 1 syringe.
Why was this product recalled?
Lack of sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on January 22, 2020. Severity: Moderate. Recall number: D-0732-2020.