AD-TECH Drill Sleeve Guides — Class II medical device recall Z-2544-2019
Terminated recall by Ad-Tech Medical Instrument Corporation, reported 2019-09-25, distributed in AZ, CA, FL, GA, IL, MA, MD, MI…. The inner diameter of the drill sleeve guide raw material was found to be under tolerance, potentially resulti
| Recall number | Z-2544-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ad-Tech Medical Instrument Corporation, Oak Creek, WI, United States |
| Recall initiated | 2019-08-27 |
| Classified | 2019-09-13 |
| Reported by FDA | 2019-09-25 |
| Terminated | 2023-04-05 |
| Distributed | AZ, CA, FL, GA, IL, MA, MD, MI, MN, NH, NY, OH, OR, PA, TX, UT, WA, WI |
| Countries outside the US | BR, CA, CZ, DK, ES, FR, GB, HK, IN, JP, KR, RU, SG, TW |
| Quantity | 315 units |
| Model numbers | DSG-6.3-090-2.4N, DSG-90-2.3N |
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
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2544-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.