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Elegance Anterior Cervical Plates
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MEDICAL DEVICE RECALLMODERATE

Elegance Anterior Cervical Plates

Clariance-SAS is recalling Elegance Anterior Cervical Plates due to the presence of burrs on the finished product.

What to do

Contact your surgeon or healthcare provider if you have concerns regarding a recent cervical procedure. Healthcare facilities should inspect their inventory and quarantine any affected plates.

Recalled
Listed
Updated
Agency
FDA
Firm
Clariance-SAS
Recall ID
98442
Status
ONGOING

Why it was recalled

Clariance-SAS is recalling various Elegance Anterior Cervical Plates due to the presence of burrs on the finished product. These implants are used for cervical spine stabilization and are distributed nationwide.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Elegance¿ Anterior Cervical Plate ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL…Model/Catalog number: See Excel sheet attached named "FDA 5072 Product Information"

UDI-DI
53430108, 03700780644353, 53430110, 03700780644353, 53430111, 03700780644384, 53430112, 03700780644391, 53430113, 03700780644407, 53430114, 03700780644414, 53430116, 03700780644438, 53430120, 03700780644452, 53430220, 03700780644452, 53430224, 03700780644490
–

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-06-11 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification