Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2372-2019 — EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903230, 14.5F, Straight ,23cm length, BARD, UDI: 00801741013706

U.S. FDA — Device Enforcement · United States · 2019-05-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2372-2019
Date of alert
2019-05-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Bard Peripheral Vascular Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00801741013706
Reported risk: The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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