Reported Apr 4, 2018 · Terminated
6F Taiga Guiding Catheter
Medtronic Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Inc · 710 Medtronic Pkwy · Minneapolis, MN · 55432-5603
Is this the product you have?
- 6F Taiga Guiding Catheter
- Lot codes and dates
- Lot/Serial Number's0008104881, 0008185945, 0008448845, 0008498609, 0008591678, 0008603130, 0008128237, 0008185937, 0008359341, 0008381347, 0008520748, 0008572204, 0008584614, 00 887489, 0008132544, 0008143685, 0008153935, 0008176874, 0008181991, 0008189749, 0008195422, 0008220305, 0008399842, 0008411526, 0008479077, 0008498645, 0008510155, 0008560305, 0008588040, 0008609897, 0008614083, 0008092512, 0008117850, 0008171020, 0008173080, 0008185946, 0008195426, 0008250618, 0008374572, 0008399835, 0008411525, 0008510141, 0008584625, 0008589932, 0008609899, 0008084699, 0008092511, 0008143683, 0008156792, 0008169119, 0008191347, 0008448842, 0008479041, 0008498608, 0008527623, 0008090683, 0008121917, 0008128241, 0008148608, 0008169116, 0008191339, 0008401589, 0008503947, 0008510133, 0008580930, 0008580935, 0008580939, 0008589915, 0008121924, 0008132534, 0008150901, 0008401588, 0008418561, 0008441398, 0008448854, 0008503956, 0008588042, 0008603140, 0008614065, 0008087481, 0008090682, 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0008448839, 0008492392, 0008498654, 0008503963, 0008535442, 0008572208, 0008586330, 0008586332, 0008589933, 0008598737, 0008603143, 0008143682, 0008171013, 0008208233, 0008448855, 0008492430, 0008506205, 0008537074, 0008562621, 0008589918, 0008603134, 0008611516, 0008084683, 0008095212, 0008121927, 0008132529, 0008156793, 0008169127, 0008189750, 0008195425, 0008216629, 0008242805, 0008351874, 0008368955, 0008374583, 0008418570, 0008441407, 0008479038, 0008506213, 0008535448, 0008551249, 0008572212, 0008589934, 0008600841, 0008611521, 0008090685, 0008128242, 0008143691, 0008165882, 0008177971, 0008399825, 0008440033, 0008471807, 0008492382, 0008506208, 0008537078, 0008582366, 0008588037, 0008603132, 0008609895, 0008090676, 0008600837, 0008621626, 0008090675, 0008479023, 0008503960, 0008548757, 0008560294, 0008582359, 0008582368, 0008603133, 0008128234, 0008490737, 0008498615, 0008584623, 0008202458, 0008441391, 0008498618, 0008140165, 0008560285, 0008140150, 0008488921, 0008104887, 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- Amount recalled
- 15,923
Why it was recalled
Stop using this product now
Complaints regarding 6F Taiga guide catheter tip detachment and/or tip splitting.
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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