PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: January 1, 2025 Initiated: November 22, 2024 #Z-0743-2025

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

Reason for Recall

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

Details

Units Affected
171 orders
Distribution
Product was distributed nationwide US, and internationally to Canada, Australia, and New Zealand.
Location
Saint Paul, MN

Frequently Asked Questions

What product was recalled?
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. Recalled by 3M Company - Health Care Business. Units affected: 171 orders.
Why was this product recalled?
Attachments may not mate with the tooth as intended in the digital treatment design.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 1, 2025. Severity: Moderate. Recall number: Z-0743-2025.