Clarity Precision Grip Attachments — Class II medical device recall Z-0743-2025
Ongoing recall by 3M Company - Health Care Business, reported 2025-01-01, distributed nationwide. Attachments may not mate with the tooth as intended in the digital treatment design.
| Recall number | Z-0743-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | 3M Company - Health Care Business, Saint Paul, MN, United States |
| Recall initiated | 2024-11-22 |
| Classified | 2024-12-20 |
| Reported by FDA | 2025-01-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, NZ |
| Quantity | 171 orders |
| UPC / GTIN / UDI-DI | 00652221307286, 00652221307293, 00652221307309, 00652221307316, 00652221307361, 00652221307378, 00652221307385, 00652221307392 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0743-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.