FDA recall Z-2442-2021

Mivi Neuroscience Inc · Class II · 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.

Reason for recall

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

Distribution

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

Key facts

Status
Terminated
Initiation date
2021-07-23
Report date
2021-09-15
Termination date
2024-05-23
Voluntary/Mandated
Voluntary: Firm initiated
Location
Eden Prairie, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2442-2021