PlainRecalls
FDA Drug Moderate Class II Terminated

TRIMIX FORTE 4 (UA) 30MG/3MG/30MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800

Reported: January 22, 2020 Initiated: December 20, 2019 #D-0777-2020

Product Description

TRIMIX FORTE 4 (UA) 30MG/3MG/30MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800

Reason for Recall

Lack of sterility assurance.

Details

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

Frequently Asked Questions

What product was recalled?
TRIMIX FORTE 4 (UA) 30MG/3MG/30MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800. Recalled by Assurance Infusion. Units affected: 10 vials.
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-0777-2020.