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FDA Medical Device Recalls (openFDA)

Heartware, Inc.: Medtronic HVAD Monitor Data Cable, Product Number: 1575

Recall number
Z-1339-2021
Recalling firm
Heartware, Inc.
Product
Medtronic HVAD Monitor Data Cable, Product Number: 1575
Status
Open, Classified
Initiated
2021-02-26
Posted
not on file
Terminated
not on file
Reason
There is the potential for the Controller power cables (AC Adapter, DC Adapter, and Battery cables), HVAD Alarm Adapter, and HVAD Monitor data cables to cause damage to the HVAD Controller ports when inserting the cables into the Controller ports, due to wear from misalignment of the cables to the port.
Root cause
Device Design
Action
The firm issued a Medical Device Notice to its consignees on 02/26/2021 by letter delivered via UPS 2-day delivery. The letter explained the issue and directed the physician to review the patient management recommendations on the frequency of of inspecting the HVAD Controller, HVAD Controller power cables, and HVAD Monitor data cables. For questions regarding this material, please contact your Medtronic Field Representative.
Quantity
1337 units (1110 US)
Distribution
Worldwide
Lot, serial or model codes
All lot codes
510(k) numbers
not on file
PMA numbers
["P100047"]
Product code
DSQ
Firm FEI
3007042319
Firm city
Miami Lakes
Firm state
FL
Firm country
not on file

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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