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.

BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This Recalled by Pacifico National, Inc. dba AmEx Pharmacy Due to Defective Delivery System: difficult to express

Date: April 19, 2019
Company: Pacifico National, Inc. dba AmEx Pharmacy
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 Pacifico National, Inc. dba AmEx Pharmacy directly.

Affected Products

BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This biologic product was repackaged by AmEx Pharmacy 1515 Elizabeth St. Suite J Melbourne, FL 32901 Lot:190212AB BUD:5/13/2019, Repackaged on 2/12/2019

Quantity: 249 syringes

Why Was This Recalled?

Defective Delivery System: difficult to express

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Pacifico National, Inc. dba AmEx Pharmacy

Pacifico National, Inc. dba AmEx Pharmacy has 5 total recalls tracked by RecallDetector.

Related Recalls

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