Ad-Tech Medical Instrument Corporation recalls
Every recall we track for Ad-Tech Medical Instrument Corporation — 14 in all, from 2017–2024 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Ad-Tech Medical Instrument Corporation peaked in 2019 (6); 14 since 2017. 7% rated “stop using now”.
All FDA recall records for Ad-Tech Medical Instrument Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 0 | 0 | 1 |
| 2019 | 0 | 2 | 2 | 2 | 6 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 3 | 0 | 3 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 2 | 1 | 0 | 3 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Ad-Tech Medical Instrument Corporation recalls
What to do if you have a recalled Ad-Tech Medical Instrument Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Ad-Tech Medical Instrument Corporation recalls
8 shown- Use cautionMedical device
Ad-Tech Medical Instrument Corporation recalls AD-TECH Spencer Probe Depth Electrode, REF SD08R-AP58X-000 8-Contact 1.12mm (A style) Depth Electrode
Ad-Tech recalls A-Style SD depth electrodes with incorrect MR safety labels. These devices may not be safe for MRI use, risking injury during scans. Affected units have specific lot numbers.
Ad-TechSep 19, 2024 - Lower riskMedical device
Ad-Tech Medical Instrument Corporation recalls Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third
Ad-Tech recalls lightweight cables with incorrect labels that could lead to improper connections. Affected items have specific lot numbers. Contact Ad-Tech for details.
Ad-TechAug 9, 2021 - Use cautionMedical device
Ad-Tech Medical Instrument Corporation recalls 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
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.
Ad-TechAug 27, 2019 - UnratedMedical device
Ad-Tech Medical Instrument Corporation recalls LSB Style Anchor Bolt. Labeled with the following parts: 13mm anodized anchor bolt body with anchor bolt cap containing
Ad-Tech recalls LSB Style Anchor Bolts sold between March 2019 and May 2019 due to non-sterile parts distributed without proper sterilization instructions, posing infection risks in surgical procedures.
Ad-TechJun 18, 2019 - Lower riskMedical device
Ad-Tech Medical Instrument Corporation recalls Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural Electrodes
Ad-Tech Medical recalls dual-sided subdural electrodes sold through May 2019 due to MR environment safety risks. These devices are approved for use in MRI but not intended for that purpose.
Ad-Tech MedicalJun 18, 2019 - Lower riskMedical device
Ad-Tech Medical Instrument Corporation recalls AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth Electrodes (Depth Electrodes, Foramen Ovale
Ad-Tech recalls Spencer Probe Depth Electrodes with incorrect contact count that may cause improper brain mapping during surgery. The recall addresses a manufacturing error where some units were labeled as 8-contact but are actually 6-contact.
Ad-TechApr 16, 2019 - Stop using nowMedical device
Ad-Tech Medical Instrument Corporation recalls AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the
Ad-Tech Medical recalls drill sleeve guides DSG-6.3-090-2.4N with specific batch numbers due to potential drill bit seizing during skull surgery. Affected units may cause serious injury.
Ad-Tech MedicalMay 2, 2018 - Lower riskMedical device
Ad-Tech Medical Instrument Corporation recalls Disposable Drill Kit which includes two drill bits, two drill stops, and two adjustment wrenches, sterile. The drill
Ad-Tech Medical recalls disposable drill kits with possible mix-up of 2.4mm and 2.8mm drill bits. These kits are used for cranial surgery and may cause errors if used incorrectly.
Ad-Tech MedicalDec 20, 2017
Ad-Tech Medical Instrument Corporation recall questions
How many recalls has Ad-Tech Medical Instrument Corporation had?
14 recalls from Ad-Tech Medical Instrument Corporation are on record with U.S. safety agencies, from 2017–2024.
What is the most recent Ad-Tech Medical Instrument Corporation recall?
Ad-Tech Medical Instrument Corporation recalls AD-TECH Spencer Probe Depth Electrode, REF SD08R-AP58X-000 8-Contact 1.12mm (A style) Depth Electrode, dated Sep 19, 2024. Every Ad-Tech Medical Instrument Corporation recall is listed on this page, newest first.
Why are Ad-Tech Medical Instrument Corporation products recalled?
The most common reasons on record: Incorrect version of labels were used. (3).
What should I do if I have a recalled Ad-Tech Medical Instrument Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Ad-Tech Medical Instrument Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.