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.

ENTYVIO 300 MG /250 ML 0.9% NACL Recalled by Infusion Options, Inc. Due to Lack of Assurance of Sterility

Date: June 12, 2019
Company: Infusion Options, Inc.
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 Infusion Options, Inc. directly.

Affected Products

ENTYVIO 300 MG /250 ML 0.9% NACL, Rx Only, Infusion Options, Inc. 5924 13the Ave, Brooklyn, NY 11219-4934, 718-283-7233

Quantity: N/A

Why Was This Recalled?

Lack of Assurance of Sterility

Where Was This Sold?

This product was distributed to 1 state: NY

Affected (1 state)Not affected

About Infusion Options, Inc.

Infusion Options, Inc. has 76 total recalls tracked by RecallDetector.

Related Recalls

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