EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle — Class II medical device recall Z-1832-2024
Ongoing recall by Cook Medical Incorporated, reported 2024-05-22. Devices may contain elevated levels of bacterial endotoxin.
| Recall number | Z-1832-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cook Medical Incorporated, Bloomington, IN, United States |
| Recall initiated | 2024-04-01 |
| Classified | 2024-05-16 |
| Reported by FDA | 2024-05-22 |
| Countries outside the US | CH, DE, GB, NL |
| Quantity | 1 units |
| Reason classes | microbial contamination, sterility |
| UPC / GTIN / UDI-DI | 00827002520127 |
| Lot numbers | C2144407, C2145003 |
| Model numbers | ECHO-HD-19-A |
Product
EchoTip¿ Ultra HD Endoscopic Ultrasound Access Needle, ECHO-HD-19-A, G52012
Reason for recall
Devices may contain elevated levels of bacterial endotoxin.
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-1832-2024. 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.