Flex-Neck Classic Peritoneal Dialysis Catheter 1 Cuff Infant Coiled — Class II medical device recall Z-1143-2018
Terminated recall by Merit Medical Systems, Inc., reported 2018-03-28. 2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product.
| Recall number | Z-1143-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Merit Medical Systems, Inc., South Jordan, UT, United States |
| Recall initiated | 2017-09-20 |
| Classified | 2018-03-20 |
| Reported by FDA | 2018-03-28 |
| Countries outside the US | AT, CH, DE, FI, GB, IE |
| Quantity | 30 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00884450305850 |
| Model numbers | CF-4235/B |
| Expiration dates | 2018-12-31 |
Product
Flex-Neck Classic Peritoneal Dialysis Catheter 1 Cuff Infant Coiled, Catalog # CF-4235/B
Reason for recall
2 Cuff catheters were incorrectly configured and labeled as 1 Cuff product.
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-1143-2018. 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.