---
title: "Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174 — FDA record Z-1039-2026 | Is It on Recall"
description: "Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant."
url: https://isitonrecall.com/recall/fda-device-z-1039-2026-medicrea-ib3d-pl-instruments-set-rx-only-ref-sps03174/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174 — FDA record Z-1039-2026

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 Oct 29, 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**: Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174
- **Reason**: Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant.
- **Classification**: Class II
- **Recalling firm**: Medicrea International
- **Quantity**: 44 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1039-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1039-2026%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 | Lot# 0001, 0002, 0003, 0004, 0005, 0006, 0008, 0009, 0010, 0011, 0012, 0013, 0014, 0016 ,0017 ,0018, 0020, 0021, 0024, 0025, 0026, 0029/UDI: SPS03174 |

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

## Distribution

US Nationwide distribution in the states of TN, CA, MN, NC, TX, FL, OH, RI, VA.

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

- [Alaska](https://isitonrecall.com/state/alaska/)
- [Alabama](https://isitonrecall.com/state/alabama/)
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- [Connecticut](https://isitonrecall.com/state/connecticut/)
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- [Hawaii](https://isitonrecall.com/state/hawaii/)
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- [North Dakota](https://isitonrecall.com/state/north-dakota/)
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- [New York](https://isitonrecall.com/state/new-york/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)
- [Oregon](https://isitonrecall.com/state/oregon/)
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- [Rhode Island](https://isitonrecall.com/state/rhode-island/)
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- [Utah](https://isitonrecall.com/state/utah/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jan 21, 2026
- **Recall initiation date**: Oct 29, 2025
- **Center classification date**: Jan 9, 2026

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-1039-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medicrea International records](https://isitonrecall.com/brand/medicrea-international/)