FDA Device recall Z-2535-2024
NavaClick Syringe and Needle, Model Number LIN02
- FDA Device
- Class III
- ongoing
- Published 2024-08-14
On 2024-08-14 the FDA classified a Class III recall of NavaClick Syringe and Needle, Model Number LIN02 by Lineage Biomedical, citing incorrect GTIN number on carton.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2535-2024 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2024-07-12 |
| Published | 2024-08-14 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Lineage Biomedical |
| Distribution | US |
Product
NavaClick Syringe and Needle, Model Number LIN02
Reason
Incorrect GTIN number on carton.
Identifiers
| code_info | Product Level Labeling Full UDI: (01)00860009080522(17)250416(10)24107. Packaging Carton Level Labeling Full UDI: (01)208600090805(17)250416(10)24107 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2535-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.