RUSCH Easy Cath Coude Kit — Class II medical device recall Z-1732-2014
Terminated recall by Teleflex Medical, reported 2014-06-18, distributed in CA, FL, OH, OK. Product was packaged with a straight catheter rather than the correct coude (curved) catheter.
| Recall number | Z-1732-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2014-05-21 |
| Classified | 2014-06-09 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2015-11-23 |
| Distributed | CA, FL, OH, OK |
| Quantity | 1,000 eaches |
| Lot numbers | 02A1402484 |
Product
RUSCH Easy Cath Coude Kit, 10 FR, Rx Only, Sterile, Distributed by: Teleflex Medical, Research Triangle Park, NC 27708. A tubular device that is inserted through the urethera and is used to pass fluids to or from urinary tracts.
Reason for recall
Product was packaged with a straight catheter rather than the correct coude (curved) catheter.
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-1732-2014. 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.