---
title: "BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD F... — FDA record Z-0151-2026 | Is It on Recall"
description: "Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infectio"
url: https://isitonrecall.com/recall/fda-device-z-0151-2026-biopro-femoral-head-ceramic-heads-28-30-product-id-description-19023-head-femoral-ceramic-28mm-3-190/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC 28MM -3 19024 HEAD FEMORA... — FDA record Z-0151-2026

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 Sep 9, 2025. 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**: BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC 28MM -3 19024 HEAD FEMORAL CERAMIC 28MM +0 19025 HEAD FEMORAL CERAMIC 32MM -3 19026 HEAD FEMORAL CERAMIC 32MM +0 19027 HEAD FEMORAL CERAMIC 32MM +3
- **Reason**: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
- **Classification**: Class II
- **Recalling firm**: BioPro, Inc.
- **Quantity**: 147 total
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0151-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0151-2026%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 | Product ID/UDI-DI 19023 M20919023 19024 M20919024 19025 M20919025 19026 M20919026 19027 M20919027 All lots, all serial numbers |

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

## Distribution

US Domestic distribution to Texas and Michigan.

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

- [Michigan](https://isitonrecall.com/state/michigan/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Oct 22, 2025
- **Recall initiation date**: Sep 9, 2025
- **Center classification date**: Oct 14, 2025

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-0151-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [BioPro, Inc. records](https://isitonrecall.com/brand/biopro-inc/)