Class II — Teleflex Medical
| Recalling firm | Teleflex |
|---|---|
| Registered facility | View this company's 9 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for product not to be sterile. |
| Product | Rusch EasyCath Kit |
| Quantity | 3,700 devices |
| Distribution | Nationwide distribution to CA, FL, IL, NC, NJ, OH, OK, TX. |
| Initiated | 2019-07-01 |
| Classified | 2019-07-26 |
| Terminated | 2021-11-04 |
| Recall number | Z-2086-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Teleflex Medical (Z-2086-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/83250/
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