# FDA recall Z-0743-2025

> **3M Company - Health Care Business** · Class II · device recall initiated 2024-11-22.

## Product

Clarity Precision Grip Attachments, for use in orthodontic treatment.    Part numbers/SKUs:    359-830  359-831  359-832  359-833  359-834  359-835  359-836  359-837

## Reason for recall

Attachments may not mate with the tooth as intended in the digital treatment design.

## Distribution

Product was distributed nationwide US, and internationally to Canada, Australia, and New Zealand.

## Key facts

- **Recall number:** Z-0743-2025
- **Recalling firm:** 3M Company - Health Care Business
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-11-22
- **Report date:** 2025-01-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0743-2025

## Citation

> AI Analytics. FDA recall Z-0743-2025. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0743-2025. Source: US FDA. Licensed CC0.

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