Class III โ€” Low Risk

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

VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due to Labeling: Not Elsewhere Classified

Date: October 4, 2023
Company: Denver Solutions, LLC DBA Leiters Health
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 Denver Solutions, LLC DBA Leiters Health directly.

Affected Products

VANCOmycin HCI PF, 1.25 g added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health, 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-028-68.

Quantity: 33,480 IV Bags

Why Was This Recalled?

Labeling: Not Elsewhere Classified

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Denver Solutions, LLC DBA Leiters Health

Denver Solutions, LLC DBA Leiters Health has 22 total recalls tracked by RecallDetector.

Related Recalls

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