Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069
FDA Recall Z-3130-2024 · Posted 2024-09-12
Recalling FirmMedtronic Xomed, Inc.
Recall StatusOpen, Classified
Product CodeEQJ
Date Initiated2024-07-05
Product Quantity1 unit
Reason for Recall
Product was distributed past expiration date.
Firm Action
Medtronic issued an URGENT: MEDICAL DEVICE RECALL notice to its sole consignee on 07/05/2024 via in person visit. The notice explained the problem, potential risk if used, and requested the product be quarantined.
Root Cause
Under Investigation by firm
Distribution Pattern
International distribution to the country of Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.