FDA recall, , Moderate risk
Clariance Elegance Anterior Cervical Plates
Elegance cervical plates have a burr on the finished product.
Summary by Recall Canary from the FDA notice
What happened
Clariance-SAS of Beaurains, France, recalled its Elegance Anterior Cervical Plate products due to a quality issue involving the presence of burr on the finished cervical plate product. The recall began on February 20, 2026, and was added to the FDA's Enforcement Report on April 15, 2026. The products were distributed in California, Illinois, New York, and Texas.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI and lot code are listed under that product.
A UDI-DI is the device identifier printed with the barcode on the device label.
Elegance¿ Anterior Cervical Plate Elegance 1 Level Cervical Plate, Elegance 2 Level Cervical Plate, Elegance 3 Level Cervical Plate, Elegance 4 Level Cervical Plate
- UDI-DI
- 53430108
- 03700780644353
- 53430110
- 53430111
- 03700780644384
- 53430112
- 03700780644391
- 53430113
- 03700780644407
- 53430114
- 03700780644414
- 53430116
- 03700780644438
- 53430120
- 03700780644452
- 53430220
- 53430224
- 03700780644490
- 53430228
- 03700780644513
- 53430230
- 03700780644520
- 53430232
- 03700780644537
- 53430234
- 03700780644544
- 53430236
- 03700780644551
- 53430240
- 03700780644575
- 53430338
- 03700780644582
- 53430344
- 03700780644605
- 53430347
- 03700780644612
- 53430350
- 03700780644629
- 53430353
- 03700780644636
- 53430356
- 03700780644643
- 53430362
- 03700780644667
- Lot code
- 5072
- PC03X
- R879X
- P758X
- RAA2X
- R825X
- R902X
- R194X
- RAA1X
- R195X
- RAB2X
- R196X
- R197X
- R584X
- RA81X
- R585X
- R586X
- R182X
- R587X
- RAA0X
- R588X
- R589X
- RA80X
- R556X
- RA99X
- R590X
- RAB3X
- R591X
- R880X
- RA98X
- R592X
- R881X
- RA97X
- RAU3X
- R593X
- RA96X
- R5B7X
- RAV7X
- R5B2X
- RAY6X
- R5B3X
- R8H4X
- RA95X
- R579X
- RA94X
- R5B0X
- R5B1X
- R5B6X
- RB63X
- R594X
- Model/Catalog number
- See Excel sheet attached named "FDA 5072 Product Information"
Recall details
- Company began the recall
- Sold in
U.S. Nationwide distribution in the states of California, Illinois, New York and Texas.
- Company
- Clariance-SASBeaurains, France
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98442
- Recall number
- Z-1821-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
