Rusch EasyCath Kit — Class II medical device recall Z-2086-2019
Terminated recall by Teleflex Medical, reported 2019-08-07, distributed nationwide. Potential for product not to be sterile.
| Recall number | Z-2086-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Morrisville, NC, United States |
| Recall initiated | 2019-07-01 |
| Classified | 2019-07-26 |
| Reported by FDA | 2019-08-07 |
| Terminated | 2021-11-04 |
| Distributed | Nationwide (US) |
| Quantity | 3,700 devices |
| Reason classes | sterility |
| Lot numbers | 74B1901676, 74C1900304 |
| Model numbers | ECK120, ECK125 |
| Expiration dates | 2022-03-01, 2022-06-01 |
Product
Rusch EasyCath Kit
Reason for recall
Potential for product not to be sterile.
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-2086-2019. 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.