---
title: "Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS — FDA record Z-0699-2024 | Is It on Recall"
description: "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."
url: https://isitonrecall.com/recall/fda-device-z-0699-2024-medtronic-ref-9733236-pin-150mm-sterile-percutaneous/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS — FDA record Z-0699-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 28, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS
- **Reason**: 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.
- **Classification**: Class II
- **Recalling firm**: Medtronic Navigation, Inc.
- **Quantity**: 4,224
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0699-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0699-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI: 00613994247865 and 00643169105669(Japan)/ Serial Numbers: 2023041143, 2023051122, 2023051457, 2023051458, 2023060918, 2023051459, 2022030438, 2023041136, 2023041141 |

Match all identifying details in the current notice. A brand name alone is not enough.

## 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.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jan 17, 2024
- **Recall initiation date**: Nov 28, 2023
- **Center classification date**: Jan 10, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0699-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medtronic Navigation, Inc. records](https://isitonrecall.com/brand/medtronic-navigation-inc/)
