FDA Device recall Z-0743-2025
Clarity Precision Grip Attachments, for use in orthodontic treatment
- FDA Device
- Class II
- ongoing
- Published 2025-01-01
On 2025-01-01 the FDA classified a Class II recall of Clarity Precision Grip Attachments, for use in orthodontic treatment by 3m Health Care Business, citing attachments may not mate with the tooth as intended in the digital treatment design.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0743-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-11-22 |
| Published | 2025-01-01 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | 3m Health Care Business |
| Distribution | US |
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
Attachments may not mate with the tooth as intended in the digital treatment design.
Identifiers
| code_info | Only 3M Clarity Precision Grip Attachment Dual Arch Attachments are potentially affected. Part numbers/UDI-DI: 359-83…Only 3M Clarity Precision Grip Attachment Dual Arch Attachments are potentially affected. Part numbers/UDI-DI: 359-830/ 00652221307286; 359-831/ 00652221307293; 359-832/00652221307309; 359-833/ 00652221307316; 359-834/ 00652221307361; 359-835/ 00652221307378; 359-836/ 00652221307385; 359-837/ 00652221307392 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0743-2025%22
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