NavaClick Syringe and Needle — Class III medical device recall Z-2535-2024
Ongoing recall by LINEAGE BIOMEDICAL, INC, reported 2024-08-14, distributed nationwide. Incorrect GTIN number on carton.
| Recall number | Z-2535-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | LINEAGE BIOMEDICAL, INC, Stuart, FL, United States |
| Recall initiated | 2024-07-12 |
| Classified | 2024-08-08 |
| Reported by FDA | 2024-08-14 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 00860009080522 |
| Model numbers | LIN02 |
Product
NavaClick Syringe and Needle, Model Number LIN02
Reason for recall
Incorrect GTIN number on 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-2535-2024. 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.