---
title: "Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Pro... — FDA record Z-1493-2026 | Is It on Recall"
description: "Behind-the-ear sound processer packaging label is different then included product."
url: https://isitonrecall.com/recall/fda-device-z-1493-2026-brand-name-hiresolution-bionic-ear-system-product-name-sky-ci-m90-sound-processor-model-catalog-numb/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor Model/Catalog Number: CI-5295-150 — FDA record Z-1493-2026

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 Nov 27, 2025. 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: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor Model/Catalog Number: CI-5295-150
- **Reason**: Behind-the-ear sound processer packaging label is different then included product.
- **Classification**: Class II
- **Recalling firm**: Advanced Bionics, LLC
- **Quantity**: 2 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1493-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1493-2026%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 | Lot Code: UDI-DI: 08400944CI5295YJ Model Number: CI-5295-150 Serial Numbers: 249596, 249603 |

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

## Distribution

Unknown

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Mar 11, 2026
- **Recall initiation date**: Nov 27, 2025
- **Center classification date**: Mar 5, 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-1493-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Advanced Bionics, LLC records](https://isitonrecall.com/brand/advanced-bionics-llc/)