Reported May 25, 2022 · Ongoing
HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420
Heartware, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Heartware, Inc. · 14400 Nw 60th Ave · Miami Lakes, FL · 33014-2807
Is this the product you have?
- HeartWare Ventricular Assist Device (HVAD) System Controller, Model Number 1420
- Lot codes and dates
- GTIN 00888707000420
- Serial Numbers
510 of 510 codes
CON301559CON301671CON301680CON301691CON301692CON301699CON301714CON301828CON302225CON302283CON302286CON302325CON303175CON303662CON303733CON303773CON304089CON304110CON304225CON304349CON300543CON300552CON300553CON300556CON300619CON300621CON300623CON300628CON300638CON300902CON301367CON301375CON301485CON301625CON301674CON301708CON301870CON301935CON301943CON301978CON301996CON302001CON302013CON302049CON302113CON302127CON302138CON302142CON302143CON302162CON302165CON302169CON302172CON302177CON302180CON302182CON302183CON302199CON302227CON302250
- Amount recalled
- 510 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Why it was recalled
Finnish and Turkish translation errors in HVAD controller and monitor displays as will as Instructions for Use, Patient Manual, and Emergency Responder Guide for the HeartWare Ventricular Assist Device (HVAD) system.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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