3M Company - Health Care Business: Device Recall
Recall #Z-0743-2025 · 11/22/2024
Class II: Risk
Recall Details
- Recall Number
- Z-0743-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- 3M Company - Health Care Business
- Status
- Ongoing
- Date Initiated
- 11/22/2024
- Location
- Saint Paul, MN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 171 orders
Reason for Recall
Attachments may not mate with the tooth as intended in the digital treatment design.
Product Description
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
Distribution Pattern
Product was distributed nationwide US, and internationally to Canada, Australia, and New Zealand.
Other Recalls by 3M Company - Health Care Business
- Class II: Risk 08/14/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.