Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

TMJ Arthroscopy Drape Recalled by Microtek Medical Inc. Due to Latex content in product was labeled incorrectly as...

Date: April 8, 2022
Company: Microtek Medical Inc.
Status: Terminated
Source: FDA (Device)

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 Microtek Medical Inc. directly.

Affected Products

TMJ Arthroscopy Drape, 85''x 96''

Quantity: 12 cases (120 drapes)

Why Was This Recalled?

Latex content in product was labeled incorrectly as latex free.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Microtek Medical Inc.

Microtek Medical Inc. has 8 total recalls tracked by RecallDetector.

Related Recalls

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