---
title: "META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690 — FDA record Z-1806-2025 | Is It on Recall"
description: "Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which woul"
url: https://isitonrecall.com/recall/fda-device-z-1806-2025-meta-tan-lag-compression-screw-kit-90mm-85mm-ref-71642690/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690 — FDA record Z-1806-2025

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 Mar 18, 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**: META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
- **Reason**: Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which would require replacement with another adequate size screw, and exchange may exceed 30 minutes.
- **Classification**: Class II
- **Recalling firm**: Smith & Nephew, Inc.
- **Quantity**: 75
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1806-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1806-2025%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: 00885556132975. Lot: 24CT81426. Expiration: 25-Mar-2034 |

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

## Distribution

Worldwide - US Nationwide distribution in the states of FL, NH, TX, CA, OH, NY, AL, IA, MA, NV, MO, WA, LA, TN, NC, KY, NM, NJ, AZ and the country of ZA.

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 28, 2025
- **Recall initiation date**: Mar 18, 2025
- **Center classification date**: May 19, 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-1806-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Smith & Nephew, Inc. records](https://isitonrecall.com/brand/smith-nephew-inc/)
