EIT CIF cage — Class II medical device recall Z-1324-2022
Ongoing recall by DePuy Spine, Inc., reported 2022-07-13, distributed nationwide. Label on the Outer Carton does not match the labels on the Outer Blister package, Inner Blister package and Pa
| Recall number | Z-1324-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Spine, Inc., Raynham, MA, United States |
| Recall initiated | 2022-05-20 |
| Classified | 2022-07-01 |
| Reported by FDA | 2022-07-13 |
| Distributed | Nationwide (US) |
| Quantity | 46 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04260557770573 |
| Lot numbers | E20CL0637 |
| Model numbers | CUI8070S |
Product
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
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1324-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.