The Recall Desk
HighFDA (Devices)·Z-2379-2019·Announced 2019-09-04

Bard Equistream XK Hemodialysis Catheter Recall for Tip Defects

Bard Peripheral Vascular Inc is recalling Equistream XK Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a structural defect (tip breakage) during a medical procedure, which poses a risk of harm even though specific injuries are not detailed in the source text.

Plain-English summary

Bard Peripheral Vascular Inc is recalling 309 units of Equistream XK Long-Term Hemodialysis Catheters with Preloaded Stylet (REF/Product code: 5913270, 16F, Straight, 27cm length). The recall is initiated due to complaints that the molded tip of the tunneler breaks or is damaged during the catheter placement procedure.

The affected units are distributed across the United States and in Australia and Canada. The specific lots involved are RECZ0638 (expiration 9/30/2020) and RECW0661 (expiration 7/31/2020). The agency has classified this as a Class II recall.

Healthcare providers and patients should stop using the affected catheters and contact Bard Peripheral Vascular Inc for further instructions or replacement.

The recalled product

Product
EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913270, 16F, Straight, 27cm length, BARD, UDI: 00801741013850
Manufacturer
Bard Peripheral Vascular Inc
Category
Medical Device — Hemodialysis Catheter
Hazard
Affected units
309

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • (Lot #
  • Exp.) RECZ0638 9/30/2020
  • RECW0661 7/31/2020

Distribution

Distributed in 53 states:

Part of a larger recall action

This product is one of 28 recalled by Bard Peripheral Vascular Inc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 28 products in this recall →

Related recalls

Same manufacturer · Bard Peripheral Vascular Inc

See all →

Same hazard · structural defect

See all →