Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Norepinephrine 8 mg (32 mcg/mL) added to 0.9% Sodium Chloride Recalled by QuVa Pharma, Inc. Due to Incorrect excipient: Product was compounded in 250 mL...

Date: November 21, 2018
Company: QuVa Pharma, Inc.
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 QuVa Pharma, Inc. directly.

Affected Products

Norepinephrine 8 mg (32 mcg/mL) added to 0.9% Sodium Chloride Injection 250 mL Bag, Rx only, Compounded by: QuVA Pharma 1075 West Park One Drive Suite 100 Sugar Land, TX 77478. Product Code 70092-9035-05

Quantity: 168 bags

Why Was This Recalled?

Incorrect excipient: Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride

Where Was This Sold?

This product was distributed to 1 state: CA

Affected (1 state)Not affected

About QuVa Pharma, Inc.

QuVa Pharma, Inc. has 37 total recalls tracked by RecallDetector.

Related Recalls

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