← Search recalls
FDA (Device enforcement)Recalled 2022-03-30class ii

Heartware, Inc.: HeartWare Ventricular Assist Device (HVAD) System, Pump Implant Kit, Model Number1104

Is my product affected?

HeartWare Ventricular Assist Device (HVAD) System, Pump Implant Kit, Model Number1104

  • UPC 00888707000598
  • UPC 00888707001649
  • UPC 00888707002424
  • UPC 00888707004558
  • UPC 00888707006323
  • UPC 00888707005951
  • UPC 00888707006347
  • UPC 00888707003209
  • UPC 00888707002486

Check against the official notice below — it lists the full affected range.

What happened

Heartware, Inc. is recalling 236 units of the HeartWare Ventricular Assist Device (HVAD) System, Pump Implant Kit, Model Number 1104, distributed in Finland and Turkey. The recall is due to translation errors in Finnish and Turkish language versions of the device's controller and monitor displays, as well as in the Instructions for Use, Patient Manual, and Emergency Responder Guide.

The affected devices are identified by specific serial numbers organized under seven different product codes (GTINs). The recall affects devices with serial numbers ranging from HW28827 through HW37154, with the complete list of affected serial numbers specified in the distribution records.

The source document does not specify a remedy for consumers who have received affected devices.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: Finland and Turkey Quantity: 236 units Lot/code info: GTIN 00888707000598, Serial Numbers: HW28827 GTIN 00888707001649, Serial Numbers: HW29474, HW29864, HW29985, HW30222, HW31506, HW31511, HW32021, HW32255, HW32301, HW34343, HW35068, HW35085, HW35290, HW35311, HW35349, HW35559, HW35657, HW35662, HW35664 GTIN 00888707002424, Serial Numbers: HW29480, HW29696, HW30650, HW30766, HW30767, HW31698, HW31851 GTIN 00888707004558, Serial Numbers: HW34759, HW34785, HW35655, HW35656 GTIN 00888707006323, Serial Numbers: HW34982, HW35722, HW36082, HW36189, HW36297, HW36375, HW36452, HW36539, HW36605, HW36649, HW36687, HW36740, HW36798, HW36865, HW37202 GTIN 00888707005951, Serial Numbers: HW35887, HW35893 GTIN 00888707006347, Serial Numbers: HW36040, HW36048, HW36049, HW36050, HW36051, HW36052, HW36053, HW36054, HW36055, HW36088, HW36089, HW36092, HW36093, HW36094, HW36095, HW36096, HW36097, HW36100, HW36101, HW36102, HW36103, HW36105, HW36106, HW36107, HW36108, HW36109, HW36110, HW36111, HW36112, HW36170, HW36540, HW36541, HW36542, HW36543, HW36544, HW36565, HW36566, HW36568, HW36569, HW36570, HW36571, HW36572, HW36573, HW36574, HW36575, HW36576, HW36577, HW36578, HW36579, HW36581, HW36582, HW36583, HW36584, HW36585, HW36586, HW36611, HW36612, HW36615, HW36616, HW36618, HW36619, HW36620, HW36621, HW36622, HW36623, HW36808, HW36809, HW36810, HW36918, HW36946, HW36948, HW36949, HW36950, HW36951, HW36952, HW36953, HW36954, HW36955, HW36956, HW36959, HW36960, HW36961, HW36962, HW36963, HW37006, HW37007, HW37008, HW37009, HW37010, HW37154, HW371

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

Related recalls

All FDA (Device enforcement) recalls

Hurt by this product? Start a free Case Check

ProductRisk is not a law firm and does not provide legal services or legal advice. ProductRisk is a free consumer product-safety information service operated by Plaintify, Inc., a technology company. If you ask to be connected with a law firm, any legal services are provided by that firm — not by ProductRisk or Plaintify.

Privacy · Plaintify