---
title: "UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, ... — FDA record Z-0458-2022 | Is It on Recall"
description: "The U-channel sheaths may cause damage to ProACT implant devices when the devices are passed through the sheath during a ProACT implantation procedure."
url: https://isitonrecall.com/recall/fda-device-z-0458-2022-uromedica-implantation-instrument-set-sheath-and-sharp-trocar-ref-750041-nonsterile/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile. — FDA record Z-0458-2022

Reported terminated

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 22, 2021. 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**: UROMEDICA Implantation Instrument Set (Sheath and Sharp Trocar), REF 750041, nonsterile.
- **Reason**: The U-channel sheaths may cause damage to ProACT implant devices when the devices are passed through the sheath during a ProACT implantation procedure.
- **Classification**: Class II
- **Recalling firm**: Uromedica Inc.
- **Quantity**: 18 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0458-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0458-2022%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 | Lot numbers UM00794 and UM00817, UDI 00180668000106 |

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

## Distribution

US Nationwide distribution in the states of AZ, CA, CO, KS, MD, TX, and WI.

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 12, 2022
- **Recall initiation date**: Nov 22, 2021
- **Center classification date**: Jan 5, 2022
- **Termination date**: Aug 11, 2023

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-0458-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Uromedica Inc. records](https://isitonrecall.com/brand/uromedica-inc/)