Ad-Tech recalls drill sleeve guides (DSG-90-2.3N, DSG-6.3-090-2.4N) sold 2014-2019 due to potential drill bit seizing during surgery. Affected users should contact Ad-Tech for details.
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.
Ad-Tech recalls specific drill sleeve guides used with their placement kits because the inner diameter may be too small, risking drill bit seizure during surgery. This could lead to complications if the drill gets stuck while operating.
The drill sleeve guides have an inner diameter smaller than intended, which can cause the drill bit to seize during surgical procedures. This might lead to the drill getting stuck, potentially causing injury or delaying surgery.
Medical professionals using Ad-Tech Placement Kits with the recalled drill sleeve guides from January 2014 to May 2019 are most at risk. Patients undergoing surgery with these tools may face complications.
Check for model numbers DSG-90-2.3N or DSG-6.3-090-2.4N on the drill sleeve guides. These were sold between January 2014 and May 2019 with Ad-Tech Placement Kits.
Identify the model number on your drill sleeve guide to see if it matches DSG-90-2.3N or DSG-6.3-090-2.4N.
Reach out to Ad-Tech Medical Instrument Corporation for instructions on how to return or replace the product.
The recalled models are DSG-90-2.3N and DSG-6.3-090-2.4N.
These were sold between January 2014 and May 2019.
Check for the model numbers DSG-90-2.3N or DSG-6.3-090-2.4N on the product, which were sold between January 2014 and May 2019.
We’ve drafted a message you can send Ad-Tech to request your refund or repair — edit it as you like.
Subject: Recall Z-2544-2019 — Ad-Tech Ad-Tech Hello, I own a Ad-Tech that is covered by recall Z-2544-2019 from Ad-Tech. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
