Medtronic Sofamor Danek USA Inc: Medical Device Recall in 2018 - (Recall #: Z-0566-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 22, 2017

Date Posted: February 21, 2018

Recall Number: Z-0566-2018

Event ID: 78839

Reason for Recall:

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.

Status: Terminated

Product Quantity: 2 units

Code Information:

UDI: 00643169363502, Lot Number EM17F015

Distribution Pattern:

MN, NC

Voluntary or Mandated:

Voluntary: Firm initiated