X-CORE 2 Ti Core — Class II medical device recall Z-0738-2023
Ongoing recall by NuVasive Inc, reported 2022-12-28, distributed nationwide. Potential that insert will be unable to disengage from the vertebral body replacement device/implant
| Recall number | Z-0738-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | NuVasive Inc, San Diego, CA, United States |
| Recall initiated | 2022-11-10 |
| Classified | 2022-12-20 |
| Reported by FDA | 2022-12-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BE, BR, CO, DE, ES, GB, IT |
| Quantity | 2,031 devices |
| UPC / GTIN / UDI-DI | 00887517424204, 00887517424211, 00887517426277, 00887517426284, 00887517434210, 00887517434227 |
| Lot numbers | 7160014, 7180016, 7180018, 7220016, 7220018, DR6624, DR6658, DR6677, DR6901, DR6957, DR6958, DR7357, DR7376, DR8110, DR8465, DR8897, DR8930, DR9443, DR9592, EM3755, EM3756, EM3757, EM3758, EM3759, EM3760, EM3761, EM3762, EM3763, EM3764, EM3765, EM3766, EM5349, EM5351, EM5352, EM5353, EM5354, EM6061, EM6062, EM6063, EM6064 and 31 more |
Product
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Reason for recall
Potential that insert will be unable to disengage from the vertebral body replacement device/implant
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-0738-2023. 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.