CLARIANCE-SAS
2 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (2)
Registered facilities (2)
- Clariance, Inc. FEI 3009962553 · TX
- CLARIANCE-SAS FEI 3008992889 · FR
Recalls & enforcement
- Class IIOngoing2026-02-20Due to a quality issue regarding the presence of burr on the finished cervical plate product.
- Class IIITerminated2019-07-01Potential for the polyaxial screw to become disassembled during implant.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “CLARIANCE-SAS — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10043711-clariance-sas/
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