Ad-Tech Medical Instrument Corporation: Medical Device Recall in 2019 - (Recall #: Z-2544-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 27, 2019

Date Posted: September 25, 2019

Recall Number: Z-2544-2019

Event ID: 83628

Reason for Recall:

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.

Status: Terminated

Product Quantity: 315 units

Code Information:

All serial numbers distributed between January 2014 and May 2019

Distribution Pattern:

NY, PA, WI, AZ, IL, CA, NH, GA, MA, MN, UT, MI, WA, FL, TX, OH, OR, PA, MD, and India, Korea, Taiwan, Canada, Hong Kong, Denmark, Russia, Singapore, Japan, Brazil. UK, Spain, Czech Republic, France

Voluntary or Mandated:

Voluntary: Firm initiated