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.

Lidocaine HCL Injection Recalled by TAILSTORM HEALTH INC Due to Subpotent Drug: reduced efficacy for epinephrine

Date: July 3, 2024
Company: TAILSTORM HEALTH INC
Status: Ongoing
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 TAILSTORM HEALTH INC directly.

Affected Products

Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2

Quantity: 12,525 10 mL vials

Why Was This Recalled?

Subpotent Drug: reduced efficacy for epinephrine

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About TAILSTORM HEALTH INC

TAILSTORM HEALTH INC has 1 total recall tracked by RecallDetector.

Related Recalls

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