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.

Leucovorin Calcium Injection USP Recalled by Ben Venue Laboratories Inc Due to Presence of Particulate Matter: visible crystalline particulates and...

Date: July 5, 2012
Company: Ben Venue Laboratories 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 Ben Venue Laboratories Inc directly.

Affected Products

Leucovorin Calcium Injection USP, single use vials, 10mg/mL; 50mL, Rx only, Manufactured by: Ben Venue Labs, Inc., Bedford, OH 44146, NDC# 55390-009-01(Bedford); NDC# 55390-826-01(Novaplus)

Quantity: 226,010 vials

Why Was This Recalled?

Presence of Particulate Matter: visible crystalline particulates and the discovery of crystalline particulate in a retain sample.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Ben Venue Laboratories Inc

Ben Venue Laboratories Inc has 6 total recalls tracked by RecallDetector.

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