---
title: "INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130D... — FDA record Z-1133-2022 | Is It on Recall"
description: "Right nails were anodized, marked, and labelled as left nails and vice versa"
url: https://isitonrecall.com/recall/fda-device-z-1133-2022-intertan-1-5-nail-13mm-x-42cm-130deg-left-intertan-1-5-nail-13mm-x-42cm-130deg-right/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right — FDA record Z-1133-2022

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 Apr 22, 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**: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
- **Reason**: Right nails were anodized, marked, and labelled as left nails and vice versa
- **Classification**: Class II
- **Recalling firm**: Smith & Nephew Orthopaedics GmbH
- **Quantity**: 17 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1133-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1133-2022%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 | Product number: 71676627 (DI: 00885556131633), Batch Number: 21LT56988; 71676628 (DI: 00885556040027), Batch number: 21LT56989 |

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

## Distribution

Distributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and internationally to Canada, Australia.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 1, 2022
- **Recall initiation date**: Apr 22, 2022
- **Center classification date**: May 25, 2022

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-1133-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Smith & Nephew Orthopaedics GmbH records](https://isitonrecall.com/brand/smith-nephew-orthopaedics-gmbh/)
