---
title: "Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05; — FDA record Z-3152-2026 | Is It on Recall"
description: "Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical."
url: https://isitonrecall.com/recall/fda-device-z-3152-2026-haylard-continuous-nerve-block-tray-model-item-number-kit-bmcn001-05/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05; — FDA record Z-3152-2026

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 Aug 10, 2026. 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**: Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;
- **Reason**: Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
- **Classification**: Class I
- **Recalling firm**: AVID Medical, Inc.
- **Quantity**: 80 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-3152-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3152-2026%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 | Model/Item Number (Kit): BMCN001-05; UDI-DI: 10809160455128; Kit Lots: 1703122, 1707656, 1708053; Recalled Sodium Chloride Ampule Lot: AB5002; |

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

## Distribution

Domestic: IL, NC, VA, WY;

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

- [Illinois](https://isitonrecall.com/state/illinois/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [Virginia](https://isitonrecall.com/state/virginia/)
- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Sep 23, 2026
- **Recall initiation date**: Aug 10, 2026
- **Center classification date**: Sep 16, 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-3152-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [AVID Medical, Inc. records](https://isitonrecall.com/brand/avid-medical-inc/)