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.

methylPREDNIsolone ACETATE Recalled by RXQ Compounding LLC Due to Lack of Assurance of Sterility; autoclave parameters were...

Date: September 25, 2017
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

methylPREDNIsolone ACETATE, 40 MG/ML INJECTION SUSPENSION, 10 ML Vial, RXQ Compounding, Athens, OH --- NDC: 70731-0936-10

Quantity: 945 vials

Why Was This Recalled?

Lack of Assurance of Sterility; autoclave parameters were not correct for one of two autoclaves used to sterilize the product.

Where Was This Sold?

This product was distributed to 6 states: FL, LA, MA, OH, PA, TX

Affected (6 states)Not affected

About RXQ Compounding LLC

RXQ Compounding LLC has 88 total recalls tracked by RecallDetector.

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