QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800
Reported: January 22, 2020 Initiated: December 20, 2019 #D-0764-2020
Product Description
QUADMIX 30MG/2MG/20MCG/100MCG/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
- 190 vials
- Distribution
- Nationwide within the United States
- Location
- Houston, TX
Frequently Asked Questions
What product was recalled? ▼
QUADMIX 30MG/2MG/20MCG/100MCG/ML INJ in 1 mL vial Assurance Infusion (713) 533-8800. Recalled by Assurance Infusion. Units affected: 190 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-0764-2020.
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