The Recall Desk
HighFDA (Devices)·Z-2392-2019·Announced 2019-09-04

Bard GlidePath Hemodialysis Catheter Recall Due to Tip Damage

Bard Peripheral Vascular Inc is recalling 887 units of GlidePath 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. The hazard involves a structural defect (tip breakage) during a medical procedure, which poses a risk of harm, but the source text does not report specific injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.

Plain-English summary

Bard Peripheral Vascular Inc is recalling 887 units of GlidePath Long-Term Hemodialysis Catheters with Preloaded stylet (REF/Product code: 5397270, 14.5F, straight, 27cm length). The recall was initiated due to complaints that the molded tip of the tunneler breaks or is damaged during the catheter placement procedure.

The affected lots are REDN1397 (exp. 3/31/2020), RECX2707 (exp. 7/31/2020), RECX1119 (exp. 3/31/2020), and RECU2783 (exp. 1/31/2020). These products were distributed to various states and territories in the United States, as well as Australia and Canada.

Healthcare providers should stop using the affected devices and contact Bard Peripheral Vascular Inc for further instructions on the recall.

The recalled product

Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397270, 14.5F, straight, 27cm length, BARD, UDI: 00801741012310
Manufacturer
Bard Peripheral Vascular Inc
Category
Medical Device — Hemodialysis Catheter
Hazard
Affected units
887

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 (5)

  • (Lot #
  • Exp.) REDN1397 3/31/2020
  • RECX2707 7/31/2020
  • RECX1119 3/31/2020
  • RECU2783 1/31/2020

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

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Same hazard · structural defect

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