US Drug Recall Register
Class II · Moderate risk Terminated Initiated Dec 20, 2019 (7 years ago)

MORPHINE 15MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of sterility assurance.

What was recalled

MORPHINE 15MG/ML INJ in 20 mL syringe Assurance Infusion (713) 533-8800

Recalling firm
Assurance Infusion
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0752-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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