---
title: "Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO — FDA record Z-1812-2026 | Is It on Recall"
description: "Due to increased in complaints their is the potential for endoscopic clipping device to malfunction."
url: https://isitonrecall.com/recall/fda-device-z-1812-2026-instinct-plus-endoscopic-clipping-device-ref-g58010-rx-only-sterile-eo/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO — FDA record Z-1812-2026

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 Mar 3, 2026. 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**: Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
- **Reason**: Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
- **Classification**: Class II
- **Recalling firm**: Wilson-Cook Medical Inc.
- **Quantity**: 713,702 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1812-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1812-2026%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 | All Lots manufactured between 9/2/2023-04/20/2025 ; UDI: (01)10827002580104 |

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

## Distribution

Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of Argentina, AUSTRALIA, AUSTRIA, BAHRAIN, BELGIUM, Brunei, Darussalam, Brazil, Canada, CANARY ISLANDS, Chile, China, Colombia, Costa Rica, CROATIA, CYPRUS, CZECH REPUBLIC, DENMARK, Egypt, FINLAND, FRANCE, GERMANY, GREECE, Guatemala, Hong Kong, HUNGARY, Indonesia, India, IRELAND, ISRAEL, ITALIA, KUWAIT, LEBANON, LUXEMBOURG, MALTA, MAYOTTE, Mexico, Macao, MOROCCO, Malaysia, NEDERLAND, NORWAY, New Zealand, OMAN, PAKISTAN, Peru, POLAND, PORTUGAL, QATAR, REUNION, ROMANIA, SAUDI ARABIA, SLOVENIA, El Salvador, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, Thailand, TURKEY, Taiwan, United Arab Emirates, 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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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Apr 22, 2026
- **Recall initiation date**: Mar 3, 2026
- **Center classification date**: Apr 13, 2026

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-1812-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Wilson-Cook Medical Inc. records](https://isitonrecall.com/brand/wilson-cook-medical-inc/)
