Class III โ€” Low Risk

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

Cefuroxime Recalled by JCB Laboratories LLC Due to Subpotent Drug: The product is sub-potent prior to...

Date: January 24, 2018
Company: JCB Laboratories LLC
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 JCB Laboratories LLC directly.

Affected Products

Cefuroxime, Ophthalmic Solution for Injection, 10 mg/mL, 0.3 mL single-use syringe. This is a Compounded Drug, Hospital & Office Use Only, Not for Resale. Fagron Sterile Services/JCB Laboratories, 7335 W. 33rd St. N., Wichita, KS 67205

Quantity: 6,510 syriges

Why Was This Recalled?

Subpotent Drug: The product is sub-potent prior to its 90-day beyond use date.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About JCB Laboratories LLC

JCB Laboratories LLC has 1 total recall tracked by RecallDetector.

Related Recalls

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