---
title: "Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-... — FDA record Z-0096-2023 | Is It on Recall"
description: "Printing error on the device, size 3 Solus Standard laryngeal mask airway has been incorrectly marked with size 4 information (includes the number 4 as a size i"
url: https://isitonrecall.com/recall/fda-device-z-0096-2023-intersurgical-solus-standard-laryngeal-mask-airway-size-3-small-adult-30-50kg-model-number-8003000/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000 — FDA record Z-0096-2023

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 Aug 29, 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**: Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000
- **Reason**: Printing error on the device, size 3 Solus Standard laryngeal mask airway has been incorrectly marked with size 4 information (includes the number 4 as a size identifier, patient weight and maximum inflation volume on the airway tube and the marking #4 on the inflation line pilot balloon) may pose health risk to the patient
- **Classification**: Class II
- **Recalling firm**: Intersurgical Inc
- **Quantity**: 340 pieces
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0096-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0096-2023%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 | UDI-DISingle unit: 5030267073511 UDI-DICase: 05030267046959 Lot code: 32204071 |

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

## Distribution

OH, TN, TX

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

- [Ohio](https://isitonrecall.com/state/ohio/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Oct 26, 2022
- **Recall initiation date**: Aug 29, 2022
- **Center classification date**: Oct 17, 2022
- **Termination date**: Oct 19, 2023

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-0096-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Intersurgical Inc records](https://isitonrecall.com/brand/intersurgical-inc/)