DePuy Spine, Inc.: Medical Device Recall in 2022 - (Recall #: Z-1323-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 20, 2022

Date Posted: July 13, 2022

Recall Number: Z-1323-2022

Event ID: 90390

Reason for Recall:

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

Status: Ongoing

Product Quantity: 61 units

Code Information:

UDI-DI: 04260557770658 Lot Number: E20CL0603

Distribution Pattern:

Distribution US Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated