---
title: "Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807 — FDA record Z-0632-2024 | Is It on Recall"
description: "One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade."
url: https://isitonrecall.com/recall/fda-device-z-0632-2024-conventional-knife-crescent-2-5mm-55-degrees-bevel-up-part-number-373807/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807 — FDA record Z-0632-2024

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 Aug 25, 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**: Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
- **Reason**: One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
- **Classification**: Class II
- **Recalling firm**: Beaver Visitec International, Inc.
- **Quantity**: 1980 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0632-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0632-2024%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 | UDI-DI: 30886158000571; Lot Number: 6054027 |

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

## Distribution

International distribution to the countries of Belgium, China, France, Germany, Greece, Italy, Jordan, Lithuania, Netherlands, Oman, Poland, Spain, Sweden.

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

## Dates in the source

- **Report date**: Jan 10, 2024
- **Recall initiation date**: Aug 25, 2023
- **Center classification date**: Jan 4, 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-0632-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Beaver Visitec International, Inc. records](https://isitonrecall.com/brand/beaver-visitec-international-inc/)