medical MODERATE Updated 2018-02-21

Medtronic Sofamor Danek USA Inc recalls Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only

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Recalled Product

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

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Hazard / Issue

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.

Issued by

FDA

Affected States: MN, NC
Lot/Code Info: UDI: 00643169363502, Lot Number EM17F015

✅ 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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