Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14 — Class II medical device recall Z-1890-2015
Terminated recall by Covidien LLC, reported 2015-07-08, distributed nationwide. Catheters may not meet antimicrobial specification
| Recall number | Z-1890-2015 |
|---|---|
| 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 | 8888145048 |
| Expiration dates | 2018-02-20 |
Product
Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888145048
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-1890-2015. 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.