FDA Device recall Z-2208-2020
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter
- FDA Device
- Class II
- terminated
- Published 2020-06-10
On 2020-06-10 the FDA classified a Class II recall of EQUISTREAM¿ XK Long-Term Hemodialysis Catheter by Bard Peripheral Vascular, citing incorrect Peel-Apart Introducer Sheath in Kit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2208-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-14 |
| Published | 2020-06-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Bard Peripheral Vascular |
| Distribution | AL, AR, AZ, CA, FL, GA, IA, ID, IL, KY, LA, MD, MN, MT, NC, NY, OR, PA, TN, TX, VA, WA, WI, WV |
Product
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913230/:(01)00801741013843; 16F
Reason
Incorrect Peel-Apart Introducer Sheath in Kit.
Identifiers
| code_info | LOT RECV3572 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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All Bard Peripheral Vascular recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2208-2020%22
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