---
title: "TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients ... — FDA record Z-1622-2024 | Is It on Recall"
description: "The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell"
url: https://isitonrecall.com/recall/fda-device-z-1622-2024-tridentii-hemi-cluster48d-indicated-for-use-in-primary-and-revision-patients-at-high-risk-of-hip-dis/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog ... — FDA record Z-1622-2024

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 Feb 27, 2024. 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**: TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients at high risk of hip dislocation Catalog Number: 702-11-48D
- **Reason**: The acetabular shell may have excessive deburring, resulting in a smooth surface on the edge of the shell
- **Classification**: Class II
- **Recalling firm**: Howmedica Osteonics Corp.
- **Quantity**: 45 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1622-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1622-2024%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: (01)07613327380903(17)290313(10) Lot Number: 14875651 15005253 16044255 |

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

## Distribution

Nationwide Foreign: Netherlands, Canada, Singapore, Spain, Sweden, UK

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

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## Dates in the source

- **Report date**: May 1, 2024
- **Recall initiation date**: Feb 27, 2024
- **Center classification date**: Apr 25, 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-1622-2024%22)

## Related records

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