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Recall Observatory FDA recall evidence

Device product

MIVI Super 90 8F Guide Catheter, 95 cm, REF MIA-9095S-IDE, For Investigational Use Only; sterile, and Super 90 8F Guide Catheter, 90 cm, REF MIA-9090S-IDE, For Investigational Use Only. Device is used to facilitate the insertion and guidance of microcatheters into a selected blood vessel in the peripheral, coronary and neuro vascular systems.

Z-2442-2021

July 23, 2021

Class II

Product summary

Firm
Mivi Neuroscience Inc
Event
Event 88408
Status
Terminated
Classification
Class II
Quantity
68 units
Official record key
device-enforcement:Z-2442-2021

Official wording

Reason: There is potential for nonsterility of product due to a possible defect in the pouch seal.

Code information: Cat #MIA-9095S-IDE - Lots M20120006, exp. 9/10/2021; and M21030007, exp. 9/10/2021. Cat. #MIA-9090S-IDE - Lot M21030006, exp. 12/10/2021, and M21010009, exp. 12/10/2021.

Distribution pattern: US Distribution to states of: FL, MA, NJ, NY, and TN; and OUS (Foreign) distribution to countries of: France, Hungary, Slovenia, and Spain.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    There is potential for nonsterility of product due to a possible defect in the pouch seal.