Medtronic recalls Ultra Round Steel Cutting Bur (REF 31313069) due to distribution past expiration date. Consumers should check product details and contact Medtronic for guidance.
“Medtronic Ultra Round Steel Cutting Bur Recall: Expired Product Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/54693-medtronic-ultra-round-steel-cutting-bur-recall-expired-product-hazard. Based on FDA recall #Z-3130-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3130-2024%22&limit=1).
The Food and Drug Administration announced on July 5, 2024, that Medtronic Xomed, Inc. is recalling one unit of the Medtronic ENT Ultra Round Steel Cutting Bur due to distribution past its expiration date.
How to tell if you have it
Brand: Medtronic
Product: Medtronic ENT Ultra Round Steel Cutting Bur
Model Number: REF 31313069
UDI/DI: 0076300004142
Lot Number: 0219937928
Quantity: 1 unit
The hazard
The product was distributed past its expiration date, according to the FDA.
Context
GovInfoNow's records show Medtronic Xomed, Inc. has had 11 other recalls since November 13, 2019. Other recent recalls of similar products include Cook Medical Multipurpose Drainage Catheter Recall (March 5, 2026), Cook Medical Wayne Pneumothorax Tray Recall (March 5, 2026), and Cook Medical Spectrum Central Venous Tray Recall (March 5, 2026).
How to tell if you have this one
Check for the model number REF 31313069 on the product. The product was distributed with UDI/DI 0076300004142 and Lot Number 0219937928.
Brand
Medtronic
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the model number REF 31313069 and UDI/DI 0076300004142 on the product.
How this recall unfolded
Recall timeline
FDA published this recall 2 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-3130-2024 (July 5, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3130-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.