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.

HEPARIN 12 Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of Assurance of Sterility: Potential leakage of...

Date: June 12, 2018
Company: Avella of Deer Valley, Inc. Store 38
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 Avella of Deer Valley, Inc. Store 38 directly.

Affected Products

HEPARIN 12,500 Units in 5% Dextrose. (Heparin Sodium, USP 12,500 Units, 5% Dextrose Inj., USP 250 mL) Volume: 252.5 mL. Single dose bag. Avella Specialty Pharmacy, 24416 N 19th Avenue Phoenix, AZ 85085. NDC 42852-745-25

Quantity: 900 bags

Why Was This Recalled?

Lack of Assurance of Sterility: Potential leakage of bags.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Avella of Deer Valley, Inc. Store 38

Avella of Deer Valley, Inc. Store 38 has 50 total recalls tracked by RecallDetector.

Related Recalls

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