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.

Povidone Iodine Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack of sterility assurance.

Date: September 18, 2019
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

Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20

Quantity: 808 droptainers

Why Was This Recalled?

Lack of sterility assurance.

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