Class III โ€” Low Risk

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

Acyclovir Oral Suspension Recalled by Hi-Tech Pharmacal Co., Inc. Due to Failed Stability Specification; product viscosity and or pH...

Date: October 28, 2013
Company: Hi-Tech Pharmacal Co., 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 Hi-Tech Pharmacal Co., Inc. directly.

Affected Products

Acyclovir Oral Suspension, USP 200 mg/5 mL, Net Wt. 16 fl oz (473 mL), Rx only, Hi-Tech Pharmacal Co, Inc. Amityville, NY 11701. NDC 50383-810-16.

Quantity: 51.948 bottles

Why Was This Recalled?

Failed Stability Specification; product viscosity and or pH are below specification.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Hi-Tech Pharmacal Co., Inc.

Hi-Tech Pharmacal Co., Inc. has 10 total recalls tracked by RecallDetector.

Related Recalls

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