---
title: "Tornado Embolization Microcoil, intended for embolization of selective vessel... — FDA record Z-1762-2025 | Is It on Recall"
description: "Cook Medical identified that devices from the affected device lots may contain the incorrectly sized embolization coil."
url: https://isitonrecall.com/recall/fda-device-z-1762-2025-tornado-embolization-microcoil-intended-for-embolization-of-selective-vessel-supply-to-arteriovenous/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations a... — FDA record Z-1762-2025

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 Apr 17, 2025. 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**: Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN MWCE-18S-3/2-TORNADO (GPN G08261), RPN MWCE-18S-3/2-TORNADO-081800 (GPN G13102), RPN MWCE-18S-4/2-TORNADO (GPN G08357)
- **Reason**: Cook Medical identified that devices from the affected device lots may contain the incorrectly sized embolization coil.
- **Classification**: Class II
- **Recalling firm**: Cook Incorporated
- **Quantity**: 2952 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1762-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1762-2025%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 | MWCE-18S-3/2-TORNADO, UDI-DI: 00827002082618, Lot Numbers: 16183145 16183146 16194351 16196532 16196533 16197253 NS16188093 NS16192163 16196534 16196535 16197247 16197248 16197249 16197250 16197251 16197252 16204238 NS16199061 16233647 16233648 16233649 NS16233646; MWCE-18S-4/2-TORNADO, UDI-DI: 00827002083578, Lot Numbers: 16178639 16181782 16181783 16181784 16186101 NS16178638; MWCE-18S-3/2-TORNADO-081800, UDI-DI: 00827002131026, Lot Numbers: 16188094 16188095 |

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

## Distribution

worldwide - No US distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: May 21, 2025
- **Recall initiation date**: Apr 17, 2025
- **Center classification date**: May 14, 2025

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-1762-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Cook Incorporated records](https://isitonrecall.com/brand/cook-incorporated/)