OFFICIAL-SOURCE RECALL · AUSTRALIA
Philips MR Systems on R11, R12.1.1, and R12.2.0 Recall: 6/10/2026 Philips MR Systems on R11, R12
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
- Philips MR Systems on R11, R12.1.1, and R12.2.0
- Manufacturer
- See official notice
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
6/10/2026 Philips MR Systems on R11, R12.1.1, and R12.2.0 Medical Device Product Correction Class III Hospital
Hazard
6/10/2026 Philips MR Systems on R11, R12.1.1, and R12.2.0 Medical Device Product Correction Class III Hospital
Official recall notice
Philips MR Systems on R11, R12.1.1, and R12.2.0
Agency: Therapeutic Goods Administration
Official publication date: October 6, 2026
Read the official AU_TGA_DRAC recall notice →SCAN ONCE. KEEP WATCHING.
Keep an eye on the products at home.
Scan food and household product barcodes, save your items and get notified when a future recall may match.
