FDA Recall Open, Classified

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

Recall: Z-0743-2025 · Initiated November 22, 2024

Recall

Recall Number
Z-0743-2025
Event Number
95828
Firm
3M Company Health Care Business 3m Center
FEI Number
2110898
Product Code
NXC
Status
Open, Classified
Root Cause
Software design (manufacturing process)
Initiated
November 22, 2024
Posted
December 23, 2024
Address
2510 Conway Ave, Bldg 275-5w-06, Saint Paul, MN, 55144-0001

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

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

Action

On November 22, 2024, the firm notified customers via URGENT Product Recall letters. Customers were informed that select grip attachments were impacted by a software nonconformance, limited to the lower arch of specific dual-arch Clarity Precision Grip Attachment orders. The firm advises that customers not use products from the identified Case IDs, and that they should dispose of affected products. Customers should complete and return the included customer product destruction form. The firm will provide replacement product. If you have additional questions or need to report an adverse event, contact the Clinician Support team (800-423-4588, option 2) or [email protected].

Distribution

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

Quantity

171 orders