# FDA recall Z-1133-2022

> **Smith & Nephew Orthopaedics GmbH** · Class II · device recall initiated 2022-04-22.

## Product

INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left   INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right

## Reason for recall

Right nails were anodized, marked, and labelled as left nails and vice versa

## Distribution

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

## Key facts

- **Recall number:** Z-1133-2022
- **Recalling firm:** Smith & Nephew Orthopaedics GmbH
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-22
- **Report date:** 2022-06-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tuttlingen, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1133-2022

## Citation

> AI Analytics. FDA recall Z-1133-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1133-2022. Source: US FDA. Licensed CC0.

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