Palindrome SI Chronic Catheter Kit 14 — Class II medical device recall Z-1850-2015
Terminated recall by Covidien LLC, reported 2015-07-08, distributed nationwide. Catheters may not meet antimicrobial specification
| Recall number | Z-1850-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien LLC, North Haven, CT, United States |
| Recall initiated | 2015-04-23 |
| Classified | 2015-06-30 |
| Reported by FDA | 2015-07-08 |
| Terminated | 2017-07-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, BE, BR, CA, CH, CL, CN, CZ, DE, DK, EC, EG, ES, FI, FR, GB, GR, IE, IL, IN, IR, IT, LU, MA, MX, MY, NL, NO, OM, PA, PH, PL, PT, SA, SE, SG, SK, TH, TR, ZA |
| Model numbers | 8888245062 |
| Expiration dates | 2018-02-20 |
Product
Palindrome SI Chronic Catheter Kit 14.5 Fr x 19cm Item Code: 8888245062 The Palindrome SI Chronic Catheter is indicated for acute and chronic hemodialysis, apheresis, and infusion.
Reason for recall
Catheters may not meet antimicrobial specification
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-1850-2015. 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.