Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

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

FDA Recall Z-0566-2018 · Posted None

Recalling FirmMedtronic Sofamor Danek USA Inc
Recall StatusTerminated
Product CodeMDM
Date Initiated2017-12-22
Date Terminated2018-07-31
Product Quantity2 units

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.

Firm Action

The firm initiated the recall by letter on 12/22/2017, requesting the return of the product.

Root Cause

Process control

Distribution Pattern

MN, NC

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑