US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jul 8, 2019 (7 years ago)

Gablofen (baclofen injection), 50 mcg/mL, Single Use Syringe, Rx only, packaged in a box…

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

Why it was recalled

Failed Impurities/Degradation Specification -This recall is being initiated as a precaution due to the presence of an unknown impurity observed during shelf life of the product.

What was recalled

Gablofen (baclofen injection), 50 mcg/mL, Single Use Syringe, Rx only, packaged in a box containing one 1 mL syringe, Distributed by: Primal Critical Care, Inc., 3950 Schelden Circle Bethlehem, PA, 18017, NDC 66794-151-01

Recalling firm
Piramal Critical Care, Inc.
NDC code
66794-151-01
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1742-2019

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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