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Recall Observatory FDA recall evidence

Device product

Guardian II Hemostasis Valve, Model 8210 and Guardian II NC Hemostasis Valve, Model FH102. Intended to maintain hemostasis during the use of diagnostic/interventional devices. The device is indicated for maintaining a seal around diagnostic/interventional devices with outside diameters up to 8.0F (2.67 mm or 0.105") during diagnostic/interventional procedures.

Z-2400-2012

August 30, 2012

Class II

Product summary

Firm
Vascular Solutions, Inc.
Event
Event 63098
Status
Terminated
Classification
Class II
Quantity
3500 units
Official record key
device-enforcement:Z-2400-2012

Official wording

Reason: Vascular Solutions, Inc., became aware of a potential problem involving pouches missing a seal from Guardian II (Model 8210) and Guardian II NC (Model FH102) Hemostasis Valve which poses a risk of product contamination.

Code information: lots 27686, 27293, 22446

Distribution pattern: Worldwide distribution: USA (nationwide) including states of: AZ, AR, CA, CT, DE, FL, GA, ID, IL IN , KY, LA,MD, MN, MO, NV, NM, NY, OH, PA, SC, TN, TX, VA, WA, and WV; and countries of: Italy and Korea. Italy, Korea

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Vascular Solutions, Inc., became aware of a potential problem involving pouches missing a seal from Guardian II (Model 8210) and Guardian II NC (Model FH102) Hemostasis Valve which poses a risk of product contamination.