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Recall Observatory FDA recall evidence

Device product

Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set, REF 5C5479

Z-0550-2024

November 15, 2023

Class II

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 93376
Status
Ongoing
Classification
Class II
Quantity
339,936 devices
Official record key
device-enforcement:Z-0550-2024

Official wording

Reason: There is to an increase in complaints related to failure alarms for Wet Cassette Integrity Test occurring on the Amia devices.

Code information: UDI/DI 0085412153186, Lot Numbers: H23F23028, H23G11054, H23F24018, H23G12029, H23F24034, H23G13100, H23F24067, H23G14074, H23F25049, H23G15048, H23F25056, H23G16038, H23F26047, H23G17051, H23F26054, H23G18067, H23F27037, H23G19115, H23F27045, H23G20055, H23F27102, H23G22069, H23F28035, H23G23067, H23F28043, H23G24107, H23F29066, H23G25047, H23F30064, H23G25096, H23G01030, H23G26094, H23G02046, H23G27100, H23G05015, H23G28082, H23G06047, H23G30054, H23G07052, H23G31110, H23G08050, H23H04032, H23G09058, H23H05039, H23G10072

Distribution pattern: Worldwide distribution - US Nationwide and the country of Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    There is to an increase in complaints related to failure alarms for Wet Cassette Integrity Test occurring on the Amia devices.

Field note

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