Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Baclofen 1 mg/ml in 40 ml NS syringe Recalled by Amerita Specialty Infusion Services Due to Lack of Assurance of Sterility

Date: December 24, 2015
Company: Amerita Specialty Infusion Services
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Amerita Specialty Infusion Services directly.

Affected Products

Baclofen 1 mg/ml in 40 ml NS syringe, FOR INTRATHECAL USE ONLY, Rx Only, Compounded by Amerita, Inc., Prescott, AZ 86305-1614

Quantity: 1 syringe

Why Was This Recalled?

Lack of Assurance of Sterility

Where Was This Sold?

This product was distributed to 1 state: AZ

Affected (1 state)Not affected

About Amerita Specialty Infusion Services

Amerita Specialty Infusion Services has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report