Ad-Tech Medical Instrument Corporation 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 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Ad-Tech Medical Instrument Corporation
Lot Codes / Batch Numbers
All serial numbers distributed between January 2014 and May 2019
Products Sold
All serial numbers distributed between January 2014 and May 2019
Ad-Tech Medical Instrument Corporation is recalling AD-TECH Drill Sleeve Guides, used with Ad-Tech Placement Kits: (a) REF DSG-90-2.3N (b) REF DSG-6.3 due to 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
The firm initiated the recall by letter on 08/27/2019. The firm requested the units be returned.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, FL, GA, IL, MD, MA, MI, MN, NH, NY, OH, OR, PA, TX, UT, WA, WI
Page updated: Jan 10, 2026