2008T BlueStar Hemodialysis Machine recallZ-1867-2024 · Fresenius Medical Care Holdings, Inc. · initiated Apr 17, 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: Device Design
What the company is doing
On April 17, 2024 IMPORTANT MEDICAL DEVICE CORRECTION letters were sent to customers. Customer actions: As per the 2008T Operators Manual P/N 490122 Rev AA: Blood Pump Rotors should be inspected for proper operation, as stated in Chapter 2: Daily preparation for treatment. If you experience a dislodged guide post sleeve, bent or loose tubing guide posts, or roller cannot move freely on your current F40015481 Rev A blood pump rotor, please contact FMCRTG Technical Support Services at 800-405-1321 for a replacement Blood Pump Rotor (Part Number, F40015481, Rev C) . Have Rotor Lot Number available when requesting a replacement. Please provide this letter to your Biomedical Technician or trained personnel. 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. Provide this Customer Notice to all those who need to be aware within your organization. Complete and return the attached reply form. Biomedical Technician/ actions: A Field Service Bulletin will be posted to fmcna.com website regarding Preventative Maintenance activities for Blood Pump Rotor Tubing Guide Inspection of the need to inspect the blood pump tubing guides during the 6-month Preventive Maintenance on all 2008 Series Hemodialysis Machines. URL: https://fmcna.com/support/product-support-documents/field-service-bulletins/ 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-1867-2024
- Status
- Open, Classified
- Initiated by the company
- Apr 17, 2024
- Posted by the FDA
- May 17, 2024
- Recalling firm
- Fresenius Medical Care Holdings, Inc.
- Quantity
- 931 units
- Product code
- KDI
- FDA submissions
- K173972, K222952, K231125
- Distribution
- US Nationwide distribution.
Product description
2008T BlueStar Hemodialysis Machine, Model 191124 with Component: Blood Pump Rotor, Model Number: F40015481 Rev A.
Code information (models, lots, serial numbers)
Show the full code information (11k characters)
Component: Model Number: F40015481 Rev A, UDI/DI: N/A, All Rev A lots. Finished Devices: Model Number: 191124, UDI/DI: 00840861102082; Serial Numbers: 0T0S252551, 0T0S252801, 0T0S252806, 1T0S255908, 1T0S256180, 0T0S251792, 0T0S251809, 0T0S251811, 0T0S252810, 0T0S251585, 0T0S251883, 0T0S251899, 1T0S256179, 1T0S256183, 1T0S256184, 1T0S256185, 1T0S256188, 1T0S256190, 1T0S256192, 1T0S256193, 1T0S256197, 1T0S256213, 1T0S256219, 1T0S256220, 1T0S256233, 1T0S256249, 1T0S256255, 1T0S256256, 1T0S256262, 1T0S256278, 1T0S256281, 1T0S256282, 1T0S256286, 2T0S264834, 2T0S264839, 2T0S264852, 2T0S264856, 3T0S272211, 3T0S274176, 3T0S274177, 3T0S274178, 3T0S274183, 3T0S274187, 3T0S274189, 3T0S274190, 3T0S274192, 3T0S274194, 3T0S274195, 3T0S274197, 3T0S274202, 3T0S274204, 3T0S274205, 3T0S274207, 3T0S274209, 1T0S255921, 1T0S255924, 1T0S255936, 1T0S255937, 0T0S252151, 0T0S252175, 0T0S252538, 0T0S252542, 0T0S252554, 0T0S252843, 1T0S255902, 1T0S255904, 1T0S255913, 1T0S255914, 1T0S255915, 1T0S255928, 1T0S255929, 1T0S255930, 1T0S255933, 0T0S251304, 0T0S251902, 0T0S251905, 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3T0S272504, 3T0S272508, 1T0S255927, 1T0S255961, 1T0S255962, 1T0S255968, 1T0S255970, 1T0S255975, 1T0S255976, 1T0S255977, 1T0S255980, 1T0S255981, 1T0S255983, 1T0S255984, 1T0S255986, 1T0S255988, 1T0S255989, 1T0S255991, 1T0S255992, 1T0S255994, 1T0S255996, 1T0S256009, 3T0S270349, 3T0S270975, 3T0S270979, 3T0S270981, 3T0S270983, 3T0S274179, 3T0S274181, 3T0S274196, 3T0S274198, 3T0S274199, 3T0S274200, 3T0S274450, 3T0S274461, 3T0S274469, 3T0S274470, 3T0S274473, 3T0S274474, 3T0S274476, 3T0S274477, 3T0S274634, 3T0S274431, 3T0S274432, 3T0S274435, 3T0S274436, 3T0S274437, 3T0S274438, 3T0S274440, 3T0S274441, 3T0S274442, 3T0S274445, 3T0S274446, 3T0S274452, 3T0S274459, 3T0S274464, 3T0S274466, 3T0S274472, 3T0S274624, 3T0S274625, 3T0S274628, 3T0S274629, 3T0S274630, 3T0S274632, 3T0S274641, 3T0S274653, 3T0S274655, 3T0S274658, 3T0S274662, 3T0S274664, 3T0S274666, 3T0S274667, 3T0S274668, 3T0S274669, 3T0S274671, 3T0S274674, 3T0S274676, 1T0S256195, 1T0S256214, 1T0S256242, 1T0S256243, 1T0S256246, 1T0S256248, 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0T0S251852, 0T0S252109, 0T0S252187, 0T0S252532, 0T0S252570, 0T0S252574, 0T0S252575, 1T0S255905, 2T0S264827, 2T0S264831, 2T0S264836, 2T0S264843, 2T0S264847, 2T0S264850, 2T0S264854, 2T0S264858, 2T0S264878, 2T0S264888, 0T0S251896, 0T0S252142, 0T0S252147, 0T0S252149, 0T0S251490, 1T0S255903, 3T0S269277.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- 2008T BlueStar Hemodialysis Machine 191124Fresenius Medical Care Holdings, Inc. · Dialyzer, high permeability with or without sealed dialysate system4 recalls32 reports
Product lines
Other devices under the same FDA submission
2 devices cleared under K173972, K222952, K231125 are not named by identifier in this recall. One submission often covers many models, so they may or may not be affected.
- 2008T BlueStar Hemodialysis Machine 191126Fresenius Medical Care Holdings, Inc. · Dialyzer, high permeability with or without sealed dialysate system5 recalls10 deaths441 reports
- 2008T BlueStar Hemodialysis Machine 191130Fresenius Medical Care Holdings, Inc. · Dialyzer, high permeability with or without sealed dialysate system4 recalls7 deaths272 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 94463).
- Z-1868-2024 · Open, Classified2008T BlueStar Hemodialysis Machine, Model 191126 with Component: Blood Pump Rotor, Model Number: F40015481 Rev A.
- Z-1869-2024 · Open, Classified2008T BlueStar Hemodialysis Machine, Model 191128 with Component: Blood Pump Rotor, Model Number: F40015481 Rev A.
- Z-1870-2024 · Open, Classified2008T BlueStar Hemodialysis Machine, Model 191130 with Component: Blood Pump Rotor, 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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