Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due to an...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ormco/Sybronendo directly.
Affected Products
SnapLink, Ref Part No. 438-2191, L6L SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx Only
Quantity: 3,632,493 brackets
Why Was This Recalled?
The action is being taken due to an increase in complaints relating to the lower buccal tube slide doors not staying close. In the event of functional failure, broken/damage buccal tubes it may cause the tooth to rotate, possibly delay treatment and inconvenience the patient and clinician. If not noticed it may extend treatment by approximately 1 -3 months.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ormco/Sybronendo
Ormco/Sybronendo has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report