DePuy Spine, Inc.: Medical Device Recalls in 2022
Updated on March 25, 2026.
According to to data from the FDA, there were 2 medical device recalls made by DePuy Spine, Inc. in 2022. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- 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
- EIT CIF cage, H 7mm, 8degree, S- 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: CUI8070S