---
title: "Mi1250 SYNCHRONY 2, Item Numbers: a) 39541, FLEXSOFT S-Vector; b) 39545, FLEX... — FDA record Z-2356-2024 | Is It on Recall"
description: "A small number of devices may have a higher probability of a crack within the internal electronics substrate which could result in a non-functional device."
url: https://isitonrecall.com/recall/fda-device-z-2356-2024-mi1250-synchrony-2-item-numbers-a-39541-flexsoft-s-vector-b-39545-flex28-s-vector-c-39547-flex26-s-v/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Mi1250 SYNCHRONY 2, Item Numbers: a) 39541, FLEXSOFT S-Vector; b) 39545, FLEX28 S-Vector; c) 39547, FLEX26 S-Vector; ... — FDA record Z-2356-2024

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 18, 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**: Mi1250 SYNCHRONY 2, Item Numbers: a) 39541, FLEXSOFT S-Vector; b) 39545, FLEX28 S-Vector; c) 39547, FLEX26 S-Vector; Cochlear Implant
- **Reason**: A small number of devices may have a higher probability of a crack within the internal electronics substrate which could result in a non-functional device.
- **Classification**: Class II
- **Recalling firm**: MED-EL Elektromedizinische Gereate, Gmbh
- **Quantity**: 7 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2356-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2356-2024%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 | a) 39541, UDI/DI 09008737395414, Serial Numbers: 859106; b) 39545, UDI/DI 09008737395452, Serial Numbers: 860731, 860782, 863380; c) 39547, UDI/DI 09008737395476, Serial Numbers: 860757, 860772, 863386 |

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

## Distribution

US, Durham, NC

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

- [North Carolina](https://isitonrecall.com/state/north-carolina/)

## Dates in the source

- **Report date**: Jul 24, 2024
- **Recall initiation date**: Apr 18, 2024
- **Center classification date**: Jul 12, 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-2356-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MED-EL Elektromedizinische Gereate, Gmbh records](https://isitonrecall.com/brand/med-el-elektromedizinische-gereate-gmbh/)