OFFICIAL-SOURCE RECALL · AUSTRALIA
OmniaSecure MRI SureScan Defibrillation Leads Recall: 17/09/2026 OmniaSecure MRI SureScan Defibrillation
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryAustraliaPublishedSeptember 17, 2026Last updatedSeptember 17, 2026Official source last checkedSeptember 24, 2026 at 7:44 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- OmniaSecure MRI SureScan Defibrillation Leads
- Manufacturer
- See official notice
- Model number
- 3930M
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
17/09/2026 OmniaSecure MRI SureScan Defibrillation Leads Medical Device Recall Class II Hospital
Hazard
17/09/2026 OmniaSecure MRI SureScan Defibrillation Leads Medical Device Recall Class II Hospital
Official recall notice
OmniaSecure MRI SureScan Defibrillation Leads
Agency: Therapeutic Goods Administration
Official publication date: September 17, 2026
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