Class II — Potential Health Hazard

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

AD-TECH Drill Sleeve Guides Recalled by Ad-Tech Medical Instrument Corporation Due to The inner diameter of the drill sleeve guide...

Date: August 27, 2019
Company: Ad-Tech Medical Instrument Corporation
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 Ad-Tech Medical Instrument Corporation directly.

Affected Products

AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits: (a) REF DSG-90-2.3N (b) REF DSG-6.3-090-2.4N

Quantity: 315 units

Why Was This Recalled?

The inner diameter of the drill sleeve guide raw material was found to be under tolerance, potentially resulting in the drill bit seizing in the guide during surgery.

Where Was This Sold?

This product was distributed to 18 states: AZ, CA, FL, GA, IL, MD, MA, MI, MN, NH, NY, OH, OR, PA, TX, UT, WA, WI

Affected (18 states)Not affected

About Ad-Tech Medical Instrument Corporation

Ad-Tech Medical Instrument Corporation has 17 total recalls tracked by RecallDetector.

Related Recalls

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