FDA Device recall Z-0566-2018
Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
- FDA Device
- Class II
- terminated
- Published 2018-02-21
On 2018-02-21 the FDA classified a Class II recall of Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only by Medtronic Sofamor Danek Usa, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0566-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-12-22 |
| Published | 2018-02-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Medtronic Sofamor Danek Usa |
| Distribution | MN, NC |
Product
Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
Reason
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.
Identifiers
| code_info | UDI: 00643169363502, Lot Number EM17F015 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0566-2018%22
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