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FDA Medical Device Recalls (openFDA)

MARVAO MEDICAL DEVICES LTD.: NexSite HD, Hemodialysis Symmetric Tip Catheter for long term use

Recall number
Z-1699-2021
Recalling firm
MARVAO MEDICAL DEVICES LTD.
Product
NexSite HD, Hemodialysis Symmetric Tip Catheter for long term use
Status
Open, Classified
Initiated
2020-02-11
Posted
not on file
Terminated
not on file
Reason
The action is to ensure consistency between the Directions for Use (DFU) in the field and the DFU on the website.
Root cause
Labeling Change Control
Action
On 02/10/2020, the firm emailed a "Direction For Use Update" Letter, to inform them that the firm has updated its Directions for Use (LS 122) from revision 01 to revision 02 and stated that the update is to provide clarification of an existing warning following a complaint where the stylet hub detached following removal without a guidewire in place. The updated DFU now includes the following statement, "The stylet is not to be removed without the guidewire in place. To remove the stylet forcibly in such cases could result in device damage". Customer are begin informed that the Recalling Firm will be removing LS 122 revision 01 which they currently have and replace it with LS 122 revision 02. This "rework" (replacement) will be conducted by the Recalling Firm's distributor DirectACCESS. The rework (replacement) will occur by the end of March 2020. A copy of the DFU is provided on the Recalling Firm's website and is also attached to the customer notification email. For questions associated with this correction - contact Recalling Firm at: Telephone number - +353 (0) 91 759 301 email - chris.davey@marvaomedical.com or, DirectACCESS at (855)210-0554 Ext 114
Quantity
292 devices
Distribution
U.S.: CO, NC, SC, TX, O.U.S.: Not provided
Lot, serial or model codes
Model Number/Product Description/Lot Number: NEXHDSY1551901/NexSite HD Symmetric Tip Catheter 19cm/51377; NEXHDSY1552301/NexSite HD Symmetric Tip Catheter 23cm/51378; NEXHDSY1555501/NexSite HD Symmetric Tip Catheter 55cm/51380; NEXHDSY1552701/NexSite HD Symmetric Tip Catheter 27cm/51435;
510(k) numbers
K173805
PMA numbers
not on file
Product code
MSD
Firm FEI
3008110587
Firm city
Dangan Galway
Firm state
not on file
Firm country
Ireland

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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