2008 Series Hemodialysis Machines recallZ-2341-2024 · Fresenius Medical Care Holdings, Inc. · initiated Jun 3, 2024
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Fresenius Medical Care Holdings, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
FDA root cause category: Component design/selection
What the company is doing
On June 3, 2024 IMPORTANT MEDICAL DEVICE CORRECTION letters were sent to consignees. Fresenius Medical Care is requesting replacement of affected Blood Pump Rotors in 2008K@HOME systems due to the patients possibly being unaware of this component failing. To order for a replacement Blood Pump Rotor (Part Number, F40015481), contact Fresenius Medical Care Customer Service at 800-227-2572, OPTION 3, o Please have Blood Pump Rotor Part Number and Lot Number available when requesting a replacement. CUSTOMER: 1. Please provide this letter to your Biomedical Technician. 2. Report any complaints or adverse events to [email protected] or FDA MedWatch at https://www.fda.gov/safety/medical-product-safety-information/medwatch-forms-fda-safety-reporting. 3. Provide this Customer Notice to all those who need to be aware within your organization. 4. Complete and return the attached reply form. For any clinical or medical questions, please contact the Global Medical Information and Education Office at 1-855-616-2309.
Recall details
- Recall number
- Z-2341-2024
- Status
- Open, Classified
- Initiated by the company
- Jun 3, 2024
- Posted by the FDA
- Jul 11, 2024
- Recalling firm
- Fresenius Medical Care Holdings, Inc.
- Quantity
- 531 units
- Product code
- KDI
- Distribution
- Domestic: Nationwide Distribution. International: Canada.
Product description
190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Code information (models, lots, serial numbers)
Show the full code information (6k characters)
Model Number: 190828; UDI/DI: 00840861100941; Serial Numbers: 2K0S179489, 3K0S184885, 3K0S185744, 1K0S172050, 1K0S172202, 1K0S171823, 1K0S172056, 3K0S185989, 3K0S186038, 4K0S190849, 4K0S191132, 1K0S171846, 4K0S192532, 4K0S192534, 4K0S192232, 4K0S191583, 2K0S180629, 3K0S185738, 4K0S190517, 1K0S171488, 1K0S172266, 4K0S192736, 3K0S185730, 3K0S185732, 3K0S185734, 3K0S185740, 3K0S186955, 3K0S187000, 4K0S190509, 4K0S190514, 4K0S190515, 4K0S190519, 4K0S190525, 4K0S190537, 4K0S191511, 4K0S191571, 4K0S191578, 4K0S192514, 4K0S192520, 4K0S192522, 4K0S192523, 4K0S192528, 4K0S192538, 4K0S192235, 4K0S192231, 4K0S192236, 4K0S192237, 2K0S180521, 2K0S180522, 2K0S180527, 3K0S186036, 3K0S182626, 3K0S182627, 3K0S182637, 3K0S182646, 3K0S184910, 3K0S185719, 3K0S185721, 3K0S185739, 3K0S185742, 3K0S186938, 3K0S186951, 3K0S186953, 3K0S186960, 3K0S186995, 3K0S186997, 4K0S190280, 4K0S191586, 4K0S191229, 4K0S191230, 4K0S191232, 4K0S191569, 4K0S191579, 4K0S191580, 4K0S192727, 4K0S192731, 2K0S179494, 2K0S179487, 3K0S182636, 4K0S192226, 4K0S192227, 4K0S192234, 4K0S192239, 4K0S192241, 4K0S192245, 3K0S186032, 3K0S184877, 3K0S184878, 3K0S184895, 3K0S185724, 3K0S185736, 3K0S186042, 3K0S186935, 3K0S186990, 4K0S190518, 4K0S190524, 4K0S191584, 4K0S192242, 4K0S192737, 3K0S182658, 4K0S191129, 4K0S191133, 4K0S192537, 4K0S192230, 2K0S180524, 2K0S180526, 3K0S185720, 2K0S180530, 2K0S180542, 4K0S190538, 4K0S191124, 3K0S184906, 4K0S191233, 3K0S185978, 3K0S186944, 2K0S181716, 3K0S182642, 3K0S185975, 2K0S180516, 3K0S186993, 2K0S179479, 2K0S180529, 2K0S180533, 2K0S179490, 3K0S182656, 3K0S184887, 3K0S182645, 3K0S182655, 2K0S179482, 2K0S179477, 3K0S182635, 3K0S185997, 3K0S186948, 3K0S184893, 4K0S191234, 1K0S172200, 2K0S179485, 1K0S171809, 4K0S191582, 1K0S171481, 3K0S182650, 3K0S186992, 3K0S182654, 3K0S185981, 3K0S186044, 1K0S172057, 4K0S191512, 3K0S185729, 3K0S185979, 3K0S182641, 3K0S182643, 3K0S184890, 4K0S192526, 4K0S192533, 4K0S192729, 4K0S192735, 1K0S171848, 1K0S172052, 3K0S185735, 3K0S184884, 3K0S184892, 1K0S171482, 4K0S191136, 4K0S191122, 4K0S191125, 4K0S191134, 4K0S191123, 4K0S191141, 4K0S192243, 4K0S192244, 4K0S192540, 4K0S190531, 3K0S184891, 3K0S185723, 3K0S185745, 3K0S185988, 3K0S186956, 3K0S187002, 1K0S171808, 4K0S190513, 3K0S185718, 4K0S190511, 4K0S190530, 3K0S182625, 2K0S181709, 2K0S181711, 3K0S186034, 3K0S186998, 3K0S186942, 1K0S172061, 1K0S171825, 1K0S171841, 1K0S171483, 1K0S171815, 2K0S179500, 2K0S181717, 3K0S186950, 3K0S185998, 3K0S184899, 4K0S192730, 4K0S190533, 3K0S185741, 3K0S186962, 4K0S190516, 3K0S185737, 3K0S185728, 4K0S192240, 4K0S192233, 3K0S185310, 2K0S180512, 2K0S180543, 4K0S190846, 3K0S185743, 1K0S172045, 3K0S184879, 3K0S184881, 3K0S184905, 3K0S186933, 2K0S179499, 2K0S179501, 2K0S181719, 3K0S187001, 3K0S186947, 3K0S185994, 3K0S185983, 1K0S172189, 3K0S184907, 3K0S185311, 3K0S184868, 3K0S186989, 3K0S186941, 4K0S192517, 1K0S171818, 4K0S191581, 1K0S171477, 1K0S171498, 2K0S181705, 4K0S192228, 1K0S171839, 1K0S171843, 3K0S186039, 4K0S191139, 4K0S191588, 1K0S171822, 1K0S171829, 2K0S181715, 3K0S182633, 3K0S182638, 3K0S186037, 4K0S190520, 2K0S180525, 2K0S180518, 3K0S185974, 1K0S171479, 3K0S184902, 1K0S171494, 3K0S184865, 3K0S184867, 3K0S184875, 3K0S184889, 3K0S185977, 3K0S185987, 3K0S185996, 3K0S182648, 2K0S181706, 1K0S172042, 3K0S185726, 3K0S186958, 4K0S192536, 3K0S185716, 4K0S192512, 4K0S192728, 1K0S171838, 2K0S181710, 3K0S185992, 4K0S190527, 4K0S190541, 2K0S180546, 3K0S186954, 3K0S182647, 3K0S184874, 3K0S185283, 4K0S190532, 4K0S190534, 3K0S182659, 1K0S171811, 1K0S171832, 1K0S171844, 3K0S186996, 3K0S186999, 3K0S185725, 3K0S185727, 3K0S185982, 4K0S190844, 4K0S190526, 4K0S191570, 1K0S171492, 3K0S186952, 1K0S171491, 3K0S182634, 2K0S181708, 3K0S186991, 3K0S186040, 3K0S185717, 1K0S172192, 2K0S179495, 3K0S182644, 4K0S190539, 4K0S190845, 4K0S190847, 4K0S192527, 1K0S172049, 3K0S182632, 3K0S182651, 3K0S186041, 2K0S179496, 3K0S186939, 4K0S192734, 3K0S185995, 4K0S191140, 3K0S184911, 1K0S172182, 4K0S191131, 4K0S191135, 2K0S181713, 4K0S191130, 3K0S184908, 4K0S192229, 4K0S190522, 1K0S172185, 4K0S192530, 2K0S180517, 2K0S180531, 4K0S190852, 4K0S190853, 2K0S179488, 4K0S191231, 3K0S184894, 2K0S179484, 3K0S182652, 3K0S182657, 4K0S192516, 4K0S190543, 1K0S172059, 1K0S172190, 3K0S184872, 3K0S182629, 3K0S185985, 3K0S186946, 4K0S190512, 1K0S172186, 1K0S172188, 1K0S171810, 1K0S171831, 1K0S171828, 1K0S171842, 3K0S185284, 3K0S185309, 3K0S185722, 3K0S184903, 4K0S190850, 3K0S185281, 3K0S186043, 3K0S184864, 1K0S171480, 3K0S182649, 3K0S185984, 4K0S190521, 4K0S190528, 4K0S190535, 4K0S190536, 4K0S190542, 4K0S192519, 4K0S192525, 4K0S192531, 1K0S172043, 1K0S172193, 2K0S179478, 2K0S179481, 4K0S191585, 4K0S192238, 4K0S192515, 4K0S192524, 3K0S182628, 2K0S179497, 3K0S182630, 3K0S186934, 1K0S171485, 3K0S185733, 3K0S186035, 4K0S192732, 3K0S185731, 1K0S171476, 1K0S172051, 3K0S182653, 3K0S182639, 4K0S192724, 4K0S192726, 1K0S171814, 4K0S190523, 4K0S190854, 4K0S190510, 4K0S191126, 4K0S191127, 1K0S171497, 3K0S182631, 1K0S171827, 3K0S184909, 1K0S171824, 1K0S171826, 1K0S171475, 1K0S171499, 2K0S179480, 2K0S179483, 2K0S180513, 2K0S180519, 3K0S186945, 3K0S186957, 3K0S186936, 3K0S186045, 2K0S181707, 2K0S181712, 2K0S181718, 1K0S171487, 3K0S186940, 3K0S186959, 3K0S185986, 3K0S185991, 4K0S190540, 2K0S180520, 2K0S180532, 2K0S180628, 4K0S190851, 4K0S191587, 3K0S185282, 3K0S186031, 2K0S181714, 3K0S184869, 3K0S184871, 3K0S184873, 3K0S184880, 3K0S184900, 3K0S184904, 3K0S184912, 3K0S184866, 3K0S184876, 3K0S184886, 3K0S184888, 3K0S184896, 3K0S184897, 3K0S184898, 3K0S185993, 3K0S186033, 4K0S192513, 4K0S192535, 4K0S191572, 4K0S190529, 1K0S171833, 1K0S171840, 3K0S185308, 1K0S171849, 1K0S172044, 4K0S192725, 4K0S192529, 2K0S180523, 4K0S191137, 3K0S186937, 3K0S186943, 3K0S186994, 1K0S172196, 1K0S172264, 1K0S172265, 1K0S172183, 1K0S172263, 1K0S171837, 1K0S171493, 1K0S172191, 1K0S172201, 1K0S171489, 1K0S171807, 1K0S172054, 1K0S172194, 1K0S172198, 1K0S171820, 1K0S172205, 1K0S171819, 1K0S171830, 1K0S171486, 1K0S171836, 2K0S179486, 2K0S179492, 2K0S179493, 2K0S179498, 1K0S171812, 1K0S171813, 1K0S171821, 1K0S172048, 1K0S172053, 1K0S172060, 1K0S172179, 1K0S172184, 1K0S172204, 1K0S171847, 1K0S172180, 1K0S172203, 1K0S172195, 1K0S172197, 1K0S171816, 1K0S171835, 1K0S172058, 1K0S172187, 1K0S172199, 3K0S184882, 3K0S184901, 3K0S184883, 3K0S185307, 3K0S185976, 4K0S191138, 4K0S190848, 4K0S191128, 4K0S192521, 3K0S182640, 1K0S171817, 3K0S185980, 3K0S186961, 3K0S186949, 4K0S191513, 1K0S171834, 2K0S179491, 4K0S192733, 4K0S192723.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- 2008® Series Hemodialysis Machines 190828Fresenius Usa, Inc. · Hemodialysis system for home use2 recalls8 reports
Product lines
Other products in the same recall event
The FDA groups related products into one recall event (event 94775).
- Z-2340-2024 · Open, Classified190904 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
- Z-2343-2024 · Open, Classified190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
- Z-2344-2024 · Open, ClassifiedRTL190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
- Z-2345-2024 · Open, ClassifiedRTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
- Z-2346-2024 · Open, ClassifiedRTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
- Z-2347-2024 · Open, ClassifiedRTLR190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood Pump Rotor spare part, Model Number: F40015481 Rev A
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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