# FDA recall Z-1323-2022

> **DePuy Spine, Inc.** · Class II · device recall initiated 2022-05-20.

## Product

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

## 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

## Distribution

Distribution US Nationwide

## Key facts

- **Recall number:** Z-1323-2022
- **Recalling firm:** DePuy Spine, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-05-20
- **Report date:** 2022-07-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Raynham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1323-2022

## Citation

> AI Analytics. FDA recall Z-1323-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1323-2022. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*