ClearanceBrief
Recall Z-2400-2012 ยท DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

Vascular Solutions, Inc.

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.

DateSep 17, 2012 (initiated Aug 30, 2012)
StatusTerminated
ReasonVascular 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.
Root causeProcess control
ActionThe firm, Vascular Solutions, sent an "URGENT - Medical Device Field Safety Notice" dated August 24, 2012 and a follow-up "Urgent Medical Device Removal - Lot Specific" letter dated August 30, 2012 to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to immediately check their inventory and to follow steps outlined in the letter which included to complete and return the "VSI Account Inventory Form" via email to: customerservice@vasc.com or fax: to (763) 656-4251. If you have specific questions or concerns regarding this matter, ple
Quantity3500 units
DistributionWorldwide 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
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K092711GUARDIAN II HEMOSTASIS VALVE
Zerusa Limited, Oct 1, 2009
K101113GUARDIAN II NC HEMOSTASIS VALVE
Zerusa Limited, May 21, 2010