medical MODERATE Updated 2017-09-13

Microvention, Inc. recalls MicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophil

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Recalled Product

MicroVention Terumo Traxcess 7 Mini Guidewire with Hydrophilic Coating, Ref GW0721006M, 1 guidewire per package, sterile, RX.

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Hazard / Issue

There is a potential for the hydrophilic coating on the guidewire to delaminate from the guidewire.

Issued by

FDA

Affected States: AZ, CA, CO, MA, MI, MN, MO, NY, OH, UT, VA, WI
Lot/Code Info: Lot numbers 17030521, 17032821, and 17041831

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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View official government recall

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