Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

Atovaquone Oral Suspension Recalled by KVK-Tech, Inc. Due to Temperature abuse: the firm received customer complaints of...

Date: July 2, 2021
Company: KVK-Tech, 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 KVK-Tech, Inc. directly.

Affected Products

Atovaquone Oral Suspension, USP, 750 mg/5 mL, 210 mL bottle, Rx Only, Mfd. By: KVK-Tech, Inc., Newtown, PA 18940, NDC 10702-223-21.

Quantity: 1,692 bottles

Why Was This Recalled?

Temperature abuse: the firm received customer complaints of unusual grittiness in the product.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About KVK-Tech, Inc.

KVK-Tech, Inc. has 13 total recalls tracked by RecallDetector.

Related Recalls

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