---
title: "Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product D... — FDA record Z-2869-2026 | Is It on Recall"
description: "Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier pac"
url: https://isitonrecall.com/recall/fda-device-z-2869-2026-intramedullary-bone-saw-blade-assembly-model-catalog-number-475630-product-description-intramedullar/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blad... — FDA record Z-2869-2026

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 Jul 1, 2026. 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**: Intramedullary Bone Saw Blade Assembly Model/Catalog Number: 475630 Product Description: Intramedullary Bone Saw Blade Assembly 14mm
- **Reason**: Zimmer Biomet is conducting a medical device recall removal for various sizes of the Intramedullary Bone Saw Blade Assembly due to potential sterile barrier packaging damage caused by an exposed saw blade.
- **Classification**: Class II
- **Recalling firm**: Biomet, Inc.
- **Quantity**: 26
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2869-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2869-2026%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 | UDI-DI (01)00887868507816(17)360221(10)67818764; Lot 67818764 Model No 475630; UDI-DI (01)00887868507816(17)360401(10)67818768; Lot 67818768 Model No 475630; UDI-DI (01)00887868507816(17)360428(10)67954534; Lot 67954534 |

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

## Distribution

Refer to the attached ZFA 2026-00096\_Initial Consignee List and ZFA 2026-00096\_Initial Distribution History containing the distribution and the identification of the affected consignees.

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

## Dates in the source

- **Report date**: Aug 12, 2026
- **Recall initiation date**: Jul 1, 2026
- **Center classification date**: Aug 3, 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-2869-2026%22)

## Related records

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