Skip to content
Recall Observatory FDA recall evidence

Device product

OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses the method of freezing point depression to measure osmolality of serum, plasma, and urine. Model/Catalog Number: OsmoPRO MAX Software Version: 1.5.0.0

Z-1696-2024

March 11, 2024

Class II

Product summary

Firm
Advanced Instruments, LLC
Event
Event 94330
Status
Ongoing
Classification
Class II
Quantity
58 units
Official record key
device-enforcement:Z-1696-2024

Official wording

Reason: System error messages may delay the ability to test patient samples and the need for frequent calibration due to results outside the expected range when testing controls.

Code information: UDI-DI: 00816068021150; Serial Numbers: 23030208A, 23050414A, 23050417A, 23010059A, 23040283A, 23010014A, 23020166A, 23040284A, 23020159A, 23050410A, 23030236A, 23020165A, 23020156A, 23020161A, 23030239A, 23030210A, 23030233A, 23030232A, 23020158A, 23030206A, 22111360A, 23020155A, 23030209A, 23040287A, 22111362A, 23020160A, 23040288A, 23010052A, 22111354A, 23010055A, 22111350A, 22111365A, 23010053A, 22111363A, 23030237A, 23010062A, 23010015A, 23030202A, 23030207A, 23040290A, 23030204A, 23020157A, 22111367A, 23020158A, 23030203A, 23030240A, 22111358A, 22111359A, 23040286A, 22111355A, 23030205A, 23020164A, 22111368A, 23030238A, 23010060A, 23010061A, 23020163A, 23010011A22111364A. All serial numbers that end in A

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Canada, Czech Republic, France, Germany, Iceland, Netherlands, South Korea, Spain, Switzerland, Taiwan.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    System error messages may delay the ability to test patient samples and the need for frequent calibration due to results outside the expected range when testing controls.

Field note

Send feedback

We'll only use this to respond to your feedback.