Z-3130-2024 Class II Ongoing
FDA device recall Z-3130-2024 was initiated by Medtronic Xomed, Inc. on July 5, 2024 and is designated Class II. Reason for recall: Product was distributed past expiration date. The recall status is ongoing. Affected quantity: 1 unit.
Recall Details
- Product Type
- Devices
- Report Date
- September 18, 2024
- Initiation Date
- July 5, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 unit
Product Description
Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069
Reason for Recall
Product was distributed past expiration date.
Distribution Pattern
International distribution to the country of Canada.
Code Information
UDI/DI 0076300004142, Lot Number 0219937928