Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY — Class I medical device recall Z-0992-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-02-05, distributed nationwide. The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the cath
| Recall number | Z-0992-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-12-31 |
| Classified | 2025-01-29 |
| Reported by FDA | 2025-02-05 |
| Distributed | Nationwide (US) |
| Quantity | 58 kits |
| UPC / GTIN / UDI-DI | 00653160312720, 00653160318012, 10653160312727, 10653160318019 |
| Lot numbers | 2024092490, 2024110190 |
| Model numbers | ART600, ART690 |
Product
Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690
Reason for recall
The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
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-0992-2025. 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.