# FDA recall Z-0698-2024

> **Medtronic Navigation, Inc.** · Class II · device recall initiated 2023-11-28.

## Product

Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS

## Reason for recall

Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove.

## Distribution

Worldwide - US Nationwide distribution in the states of AK, AL, AZ, CA and the countries of Armenia, Australia, Austria, Belgium, Canada, China, Denmark, Finland, France, Germany, Hong Kong, Hungary, Ireland, Israel, Italy, Japan, Luxembourg, Netherlands, New Zealand, Oman, Portugal, Spain, Switzerland, United Kingdom.

## Key facts

- **Recall number:** Z-0698-2024
- **Recalling firm:** Medtronic Navigation, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-11-28
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lafayette, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0698-2024

## Citation

> AI Analytics. FDA recall Z-0698-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0698-2024. Source: US FDA. Licensed CC0.

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