EQUISTREAM¿ XK Long-Term Hemodialysis Catheter — Class II medical device recall Z-2208-2020
Terminated recall by Bard Peripheral Vascular Inc, reported 2020-06-10, distributed in AL, AR, AZ, CA, FL, GA, IA, ID…. Incorrect Peel-Apart Introducer Sheath in Kit.
| Recall number | Z-2208-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Peripheral Vascular Inc, Tempe, AZ, United States |
| Recall initiated | 2019-06-14 |
| Classified | 2020-06-02 |
| Reported by FDA | 2020-06-10 |
| Terminated | 2024-09-18 |
| Distributed | AL, AR, AZ, CA, FL, GA, IA, ID, IL, KY, LA, MD, MN, MT, NC, NY, OR, PA, TN, TX, VA, WA, WI, WV |
| Quantity | 215 |
| UPC / GTIN / UDI-DI | 00801741013843 |
| Lot numbers | RECV3572 |
Product
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Reason for recall
Incorrect Peel-Apart Introducer Sheath in Kit.
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-2208-2020. 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.