# FDA recall Z-2544-2019

> **Ad-Tech Medical Instrument Corporation** · Class II · device recall initiated 2019-08-27.

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2544-2019
- **Recalling firm:** Ad-Tech Medical Instrument Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-27
- **Report date:** 2019-09-25
- **Termination date:** 2023-04-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Oak Creek, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2544-2019

## Citation

> AI Analytics. FDA recall Z-2544-2019. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-2544-2019. Source: US FDA. Licensed CC0.

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