---
title: "Summit Medical Nasal Septal Button, Medium, 5cm, REF SP-78105, sterile. — FDA record Z-1171-2023 | Is It on Recall"
description: "Sterile product pouches were not sealed."
url: https://isitonrecall.com/recall/fda-device-z-1171-2023-summit-medical-nasal-septal-button-medium-5cm-ref-sp-78105-sterile/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Summit Medical Nasal Septal Button, Medium, 5cm, REF SP-78105, sterile. — FDA record Z-1171-2023

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 Jan 13, 2023. 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**: Summit Medical Nasal Septal Button, Medium, 5cm, REF SP-78105, sterile.
- **Reason**: Sterile product pouches were not sealed.
- **Classification**: Class II
- **Recalling firm**: Summit Medical, LLC
- **Quantity**: 30 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1171-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1171-2023%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 | Lot #219349, Exp. 2027-11-01, UDI (01)00385640065214(17)271101(10)219340 |

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

## Distribution

US Distribution was made to CO, FL, GA, LA, MA, and ME. There was no government/military distribution. OUS Foreign distribution was made to Canada.

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

- [Colorado](https://isitonrecall.com/state/colorado/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Louisiana](https://isitonrecall.com/state/louisiana/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)

## Dates in the source

- **Report date**: Mar 8, 2023
- **Recall initiation date**: Jan 13, 2023
- **Center classification date**: Feb 24, 2023
- **Termination date**: Aug 14, 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-1171-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Summit Medical, LLC records](https://isitonrecall.com/brand/summit-medical-llc/)