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FDAMay 20, 2022device

EIT CIF cage, H 6mm, 8degree, L- an intervertebral body fusion devices indicated for use with autograft when used as an adjunct to fusion in patients with cervical disc disease (DDD). Part Number: CUI8060L

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

The hazard

Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Patient Labels. The only label that may not be correct is on the Outer Carton

What to do

FDA enforcement status: Ongoing

Brands named

depuy spinedepuy

UPCs

04260557770658

Recall history

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

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