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.

Ascorbic Acid 400 MG/ML (Non-Corn) Injection Solution Recalled by RXQ Compounding LLC Due to Crystallization

Date: June 19, 2019
Company: RXQ Compounding LLC
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 RXQ Compounding LLC directly.

Affected Products

Ascorbic Acid 400 MG/ML (Non-Corn) Injection Solution, 65 mL per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0914-65

Quantity: N/A

Why Was This Recalled?

Crystallization

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About RXQ Compounding LLC

RXQ Compounding LLC has 88 total recalls tracked by RecallDetector.

Related Recalls

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