---
title: "32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032 — FDA record Z-0644-2022 | Is It on Recall"
description: "There is a potential for the outer Tyvek lid to de-bond from the sealed package."
url: https://isitonrecall.com/recall/fda-device-z-0644-2022-32mm-4-v40-taper-vit-head-catalog-number-6260-5-032/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# 32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032 — FDA record Z-0644-2022

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 Dec 21, 2021. 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**: 32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
- **Reason**: There is a potential for the outer Tyvek lid to de-bond from the sealed package.
- **Classification**: Class II
- **Recalling firm**: Howmedica Osteonics Corp.
- **Quantity**: 8 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0644-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0644-2022%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: 07613327012842; Lot Number: 87327407 |

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

## Distribution

Worldwide distribution - US Puerto Rico and the countries of Canada, and Malaysia.

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

## Dates in the source

- **Report date**: Feb 23, 2022
- **Recall initiation date**: Dec 21, 2021
- **Center classification date**: Feb 16, 2022

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-0644-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Howmedica Osteonics Corp. records](https://isitonrecall.com/brand/howmedica-osteonics-corp/)