FDAJanuary 17, 2020device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

ormco sybronendoormcoormco sybronendo

UPCs

0088998900265200889989002669

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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