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Recall Observatory FDA recall evidence

Device product

AxiEM" Non-Invasive Patient Tracker

Z-1039-2023

December 15, 2022

Class II

Product summary

Firm
Medtronic Navigation, Inc.
Event
Event 91354
Status
Ongoing
Classification
Class II
Quantity
1,867 devies
Official record key
device-enforcement:Z-1039-2023

Official wording

Reason: Due to increasing complaint trend for the Non-Invasive Patient Tracker system where complaints analysis indicates that users are unable to successfully verify their navigation instruments during image-guided surgery.

Code information: Product Number/CFN: 9734887XOM UDI-Device Identifier (GTIN/UPN): 00763000588380 Lot Number: 220728I 220729 Product Number/CFN: 9734887XOM UDI-Device Identifier (GTIN/UPN): 00643169608252 Lot Number: 220728I

Distribution pattern: Worldwide - U.S. distribution including in the states of AL, AR, AZ, CA, CO, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WV. The country of Japan.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Due to increasing complaint trend for the Non-Invasive Patient Tracker system where complaints analysis indicates that users are unable to successfully verify their navigation instruments during image-guided surgery.