Reported Feb 21, 2018 · Terminated

Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only

Medtronic Sofamor Danek USA Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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 Sofamor Danek USA Inc · 1800 Pyramid Pl · Memphis, TN · 38132-1703

Is this the product you have?

  • Medtronic ANGLED DRILL, REF 6630902
  • QTY1 EA Rx only
Lot codes and dates
  • UDI
    • 00643169363502
    • Lot Number EM17F015
Amount recalled
2 units

Where it was sold

Why it was recalled

Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than what is indicated on the print specification.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 31, 2018 · Data as of Sep 19, 5:30 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.