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Recall Observatory FDA recall evidence

Device product

BIOPHEN UFH Control C1, REF 224101

Z-1189-2019

March 19, 2019

Class III

Product summary

Firm
Aniara Diagnostica LLC
Event
Event 82468
Status
Terminated
Classification
Class III
Quantity
41 units
Official record key
device-enforcement:Z-1189-2019

Official wording

Reason: The manufacturer packaged incorrect versions of the Instructions for Use into specific lots for three device product codes.

Code information: Lots F1700314P2, F1700314P3, F1700314P4, F1801638P1

Distribution pattern: Distributed to accounts in MI and PA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The manufacturer packaged incorrect versions of the Instructions for Use into specific lots for three device product codes.