FDAJune 20, 2022device

Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4; Simplify Disc Size 2, Ht 5/MD-5; Simplify Disc Size 2, Ht 5, 5/MD-5L; Simplify Disc Size 2, Ht 6/MD-6; Simplify Disc Size 2, Ht 6, 5/MD-6L; Simplify Disc Size 3, Ht 5/LG-5; Simplif...

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

The hazard

Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect GTIN human readable text, which could lead to selecting an incorrectly sized unit.

What to do

FDA enforcement status: Ongoing

Brands named

nuvasive

UPCs

843285100023843285100047843285100061843285100078843285100085843285100092843285100108843285100115843285100122843285100139

Recall history

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

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