BRANMOOR
THURSDAY · 14 MAY 2026

FDA Device Recall Z-1266-2022

Medtronic Inc · Minneapolis, MN

Class I — life-threatening Ongoing

Highest impact — Class I device recall — FDA determination that use of, or exposure to, the device will cause serious adverse health consequences or death. Distribution is nationwide and the recall remains in progress.

Device

HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.

Lot / serial / GTIN: GTIN 00888707008778. Serial numbers BAT935012, BAT935059, BAT935008, BAT935009, BAT935018, BAT935020, BAT935022, BAT935023, BAT935047, BAT934999, BAT935003, BAT935010, BAT935329, BAT934928, BAT934934, BAT935160, BAT935078, BAT934997, BAT935027, BAT935048, BAT934953, BAT934933, BAT934948, BAT934853, BAT934854, BAT934858, BAT934895, BAT934899, BAT934901, BAT934903, BAT934904, BAT934905, BAT934927, BAT934932, BAT934935, BAT934940, BAT934979, BAT934981, BAT935109, BAT935112, BAT935116, BAT935117, BAT935120, BAT935122, BAT935124, BAT935127, BAT935132, BAT935133, BAT935134, BAT935136, BAT934846, BAT934848, BAT934849, BAT934850, BAT935137, BAT935142, BAT935143, BAT935145, BAT935146, BAT935148, BAT935150, BAT935151, BAT935152, BAT935154, BAT935155, BAT935156, BAT935157, BAT935158, BAT935161, BAT935162, BAT935163, BAT935164, BAT935260, BAT935301, BAT935302, BAT935303, BAT935201, BAT935202, BAT935203, BAT935172, BAT935173, BAT935174, BAT935175, BAT935176, BAT935177, BAT935178, BAT935179, BAT935180, BAT935181, BAT935182, BAT935183, BAT935184, BAT935185, BAT935186, BAT935187, BAT934910, BAT934912, BAT934914, BAT934915, BAT934916, BAT934919, BAT935317, BAT935318, BAT935319, BAT935320, BAT935322, BAT935324, BAT935217, BAT935264, BAT935269, BAT935276, BAT935277, BAT935282, BAT935283, BAT935285, BAT935286, BAT935287, BAT935312, BAT935313, BAT935314, BAT935188, BAT935189, BAT935190, BAT935191, BAT935192, BAT935193, BAT935194, BAT935195, BAT935196, BAT935197, BAT935198, BAT935199, BAT934851, BAT934852, BAT934855, BAT934857, BAT934859, BAT934861, BAT934862, BAT934863, BAT934865, BAT934866, BAT935207, BAT935210, BAT935222, BAT935256, BAT935257, BAT935230, BAT935231, BAT935233, BAT935234, BAT935236, BAT935237, BAT935238, BAT935268, BAT935270, BAT935271, BAT935272, BAT935273, BAT935275, BAT935279, BAT935280, BAT935288, BAT935290, BAT935291, BAT935292, BAT935284, BAT934844, BAT935229, BAT934917, BAT934918, BAT934920, BAT934924, BAT935232, BAT935235, BAT935247, BAT935261, BAT934867, BAT934868, BAT935265, BAT935266, BAT935204, BAT935205, BAT935206, BAT935212, BAT935213, BAT935216, BAT935250, BAT935251, BAT935252, BAT935253, BAT935254, BAT935267, BAT934869, BAT935200, BAT935262, BAT935218, BAT935219, BAT935227, BAT935228, BAT934871, BAT934873, BAT934874, BAT934875, BAT934876, BAT934877, BAT934878, BAT934880, BAT934881, BAT934882, BAT934883, BAT934884, BAT934886, BAT934909, BAT935138, BAT935140, BAT935293, BAT935294, BAT935296, BAT935259, BAT935297, BAT935298, BAT935299, BAT935300, BAT934894, BAT935326, BAT935331, BAT934982, BAT934987, BAT934988, BAT934989, BAT935032, BAT935038, BAT935039, BAT935040, BAT935042, BAT935043, BAT935051, BAT935068, BAT935074, BAT935085, BAT935089, BAT935093, BAT935094, BAT935095, BAT935098, BAT935099, BAT935100, BAT935101, BAT935102, BAT935103, BAT935104, BAT935105, BAT935106, BAT935107, BAT935108, BAT935141, BAT935144, BAT935147, BAT935149, BAT935159, BAT935165, BAT935166, BAT935167, BAT935168, BAT935169, BAT935170, BAT935171, BAT935258, BAT934887, BAT934889, BAT934891, BAT934893, BAT934870, BAT935239, BAT935240, BAT935241, BAT935242, BAT935243, BAT935244, BAT935245, BAT935246, BAT935248, BAT935249, BAT934906, BAT934908, BAT935033, BAT935036, BAT935044, BAT935017, BAT935045, BAT935001, BAT935026, BAT935114, BAT935118, BAT935121, BAT935123, BAT935263, BAT935274, BAT935278, BAT935281, BAT935315, BAT935084, BAT935086, BAT934896, BAT934897, BAT934898, BAT934949, BAT934950, BAT935323, BAT935325, BAT935327, BAT935328, BAT935330, BAT935332, BAT935005, BAT935006, BAT935025, BAT935062, BAT935064, BAT935065, BAT935208, BAT934922, BAT934926, BAT934929, BAT934930, BAT934942, BAT934943, BAT934944, BAT934945, BAT934955, BAT934959, BAT934961, BAT934964, BAT934967, BAT934968, BAT934969, BAT934970, BAT934976, BAT934977, BAT934978, BAT935002, BAT935014, BAT935049, BAT934973, BAT934974, BAT935087, BAT935091, BAT935097, BAT934962, BAT935041, BAT935046, BAT935050, BAT935053, BAT935057, BAT935058, BAT935061, BAT935063, BAT935067, BAT935071, BAT935077, BAT935080, BAT935081, BAT935088, BAT935090, BAT935092, BAT934952, BAT934954, BAT934958, BAT934921, BAT934923, BAT934925, BAT934931, BAT934941, BAT934951, BAT935015, BAT935016, BAT935019, BAT935021, BAT935096, BAT935111, BAT934998, BAT934956, BAT935024, BAT935028, BAT935034, BAT935037, BAT935069, BAT935070, BAT935215, BAT935321, BAT935135, BAT935029, BAT935030, BAT935031, BAT934946, BAT934983, BAT934984, BAT934986, BAT934992, BAT934971, BAT934972, BAT934975, BAT934980, BAT934995, BAT935000, BAT935007, BAT935013, BAT934947, BAT934996, BAT935011, BAT935052, BAT935054, BAT935056, BAT935082, BAT935072, BAT935073, BAT935075, BAT935076, BAT935004, BAT934990, BAT934991, BAT934993, BAT934994, BAT935079, BAT934985, BAT934963, BAT934965, and BAT934966. Expiration date 30-APR-22.

Quantity: 429 batteries

Reason for recall

Batteries for the HVAD system have a weld defect affecting internal components within the HVAD battery, resulting in the battery to malfunction and no longer provide power or prevent the battery from holding a complete charge or properly recharging.

Recall record

Recall number
Z-1266-2022
Classification
Class I
Status
Ongoing
Voluntary or mandated
Voluntary: Firm initiated
Firm notification
Letter
Distribution
Worldwide Distribution. US nationwide, Austria, Belgium, Finland, France, Germany, Hungary, Italy, Netherlands, New Zealand, North Macedonia, Norway, Poland, Spain, Switzerland, and the United Kingdom.
Recall initiated
2022-05-05
Classified by FDA Center
2022-06-21
FDA published
2022-06-29
Recalling firm
Medtronic Inc
Firm location
Minneapolis, MN

Operational response

A Class I device recall indicates a strong likelihood of serious adverse health consequence or death from continued use. Identify affected units by serial number, lot, or GTIN against your inventory and against implanted-device patient registry. Pull affected inventory from active use immediately. For implanted devices, follow the recalling firm’s patient-notification protocol; in most cases this requires informing affected patients and their treating physicians directly.

For the official FDA enforcement record, see FDA's Recall Search.

‹ All device recalls