---
title: "EasyFuse Dynamic Compression System Instrument Pack — FDA record Z-0853-2022 | Is It on Recall"
description: "The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking."
url: https://isitonrecall.com/recall/fda-device-z-0853-2022-easyfuse-dynamic-compression-system-instrument-pack/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# EasyFuse Dynamic Compression System Instrument Pack — FDA record Z-0853-2022

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 Mar 10, 2022. 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**: EasyFuse Dynamic Compression System Instrument Pack
- **Reason**: The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.
- **Classification**: Class II
- **Recalling firm**: Wright Medical Technology, Inc.
- **Quantity**: 176 packs
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0853-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0853-2022%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 | Model Number FFSP1530, UDI: 00889797103565 Lot Codes (Expiration Date): 781853-110321 (11/03/2029) and 780395-112221 (12/03/2029) |

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

## Distribution

US distribution to Florida, North Carolina, Ohio, and Texas

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

- [Florida](https://isitonrecall.com/state/florida/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Apr 6, 2022
- **Recall initiation date**: Mar 10, 2022
- **Center classification date**: Mar 31, 2022
- **Termination date**: Apr 1, 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-0853-2022%22)

## Related records

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