---
title: "Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusa... — FDA record Z-0521-2025 | Is It on Recall"
description: "Due to pin coming off of handles."
url: https://isitonrecall.com/recall/fda-device-z-0521-2025-brand-name-mst-duet-reusable-handle-for-single-use-heads-product-name-reusable-handle-for-single-use/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps... — FDA record Z-0521-2025

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 Sep 17, 2024. 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**: Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps and Scissors) Model/Catalog Number: DFH-1028 Software Version: N/A Product Description: A MST Single Use Forceps or Scissors System consists of a reusable handle and one of a number of single use interchangeable heads. MST Single Use Forceps and Scissor heads are shipped ready to use sterile in a tray with Tyvek lid within a sterile pouch. MST Duet Reusable Handle for Single Use Forceps & Scissor Heads are supplied in a non-sterile condition and must be sterilized prior to and after every use. The blue sleeve the handle is packaged in is not intended to be sterilized and does not maintain sterility. Component: Yes. The MST Duet¿ Reusable Handle for Single Use Heads is the reusable handle component which connect to either Single Use Forceps or Scissors heads.
- **Reason**: Due to pin coming off of handles.
- **Classification**: Class II
- **Recalling firm**: MicroSurgical Technology Inc
- **Quantity**: 24
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0521-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0521-2025%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 | Lot Code: Product Codes: HNF or HNR (Regulation Number 886.4350). Either code can apply as the Duet Handle Assembly can be used with MST Duet Ophthalmic Scissors or MST Duet Forceps. UDI: 00844685005536 Lot #: 160458. Lot number is a sequential number generated through the internal SAP. All finished goods can be effectively traced by the lot number as either the finished good part or the sub part used. Expected life: The number of handle reprocessing cycles is not limited as long as the post-cleaning and pre-use inspections determine that the product is still functional and shows no signs of damage or corrosion. |

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

## Distribution

U.S.: CT, GA, MN, MT and TX. O.U.S.: Netherlands 24 total devices = 6 devices distributed in the United States and 18 devices distributed in Germany.

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

- [Connecticut](https://isitonrecall.com/state/connecticut/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Montana](https://isitonrecall.com/state/montana/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Dec 4, 2024
- **Recall initiation date**: Sep 17, 2024
- **Center classification date**: Nov 22, 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-0521-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MicroSurgical Technology Inc records](https://isitonrecall.com/brand/microsurgical-technology-inc/)