---
title: "PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK — FDA record Z-1225-2022 | Is It on Recall"
description: "One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body."
url: https://isitonrecall.com/recall/fda-device-z-1225-2022-profemur-plasma-z-classic-stem-size-7-standard-short-neck/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK — FDA record Z-1225-2022

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 May 4, 2022. 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**: PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK
- **Reason**: One manufacturing lot is missing the plasma-spray coating in the proximal region of the stem body.
- **Classification**: Class II
- **Recalling firm**: MicroPort Orthopedics Inc.
- **Quantity**: 8 units
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-1225-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1225-2022%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 | Catalog Number(s): PHAPCLS7; Lot Number(s): 1903727; Expiration Date: 11/24/2029; UDI/DI Number: 00192629112773 |

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

## Distribution

Worldwide distribution - US Nationwide distribution in the states of FL, IN, MO, CA and the country of Canada.

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**: Jun 8, 2022
- **Recall initiation date**: May 4, 2022
- **Center classification date**: Jun 2, 2022
- **Termination date**: Jan 16, 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-1225-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MicroPort Orthopedics Inc. records](https://isitonrecall.com/brand/microport-orthopedics-inc/)
