OFFICIAL-SOURCE RECALL · AUSTRALIA
LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial) Recall: 3/09/2026 LEO+ Self-Expanding
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial) and Eclipse Balloon Catheter (Catheter, intravascular, occluding)
- Manufacturer
- See official notice
- Lot number
- cannot
The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
3/09/2026 LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial) and Eclipse Balloon Catheter (Catheter, intravascular, occluding) Medical Device Recall Class II Hospital
Hazard
3/09/2026 LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial) and Eclipse Balloon Catheter (Catheter, intravascular, occluding) Medical Device Recall Class II Hospital
Official recall notice
LEO+ Self-Expanding Nitinol Stent (Stent, vascular, intracranial) and Eclipse Balloon Catheter (Catheter, intravascular, occluding)
Agency: Therapeutic Goods Administration
Official publication date: September 3, 2026
Read the official AU_TGA_DRAC recall notice →SCAN ONCE. KEEP WATCHING.
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