PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: February 21, 2018 Initiated: December 22, 2017 #Z-0566-2018

Product Description

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

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.

Details

Units Affected
2 units
Distribution
MN, NC
Location
Memphis, TN

Frequently Asked Questions

What product was recalled?
Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only. Recalled by Medtronic Sofamor Danek USA Inc. Units affected: 2 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 21, 2018. Severity: Moderate. Recall number: Z-0566-2018.