OFFICIAL-SOURCE RECALL · AUSTRALIA
Philips BV Pulsera and Zenition Systems Recall: 24/09/2026 Philips BV Pulsera and Zenition Systems
Use the identifiers printed on your item to determine whether this recall may affect the product you own.
CountryAustraliaPublishedSeptember 24, 2026Last updatedSeptember 24, 2026Official source last checkedOctober 7, 2026 at 7:44 PM UTC
CHECK THE ITEM YOU OWN
Is your product affected?
- Brand
- See official notice
- Product
- Philips BV Pulsera and Zenition Systems
- Manufacturer
- See official notice
- Model number
- 718095, 718133
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
24/09/2026 Philips BV Pulsera and Zenition Systems Medical Device Product Correction Class I Hospital
Hazard
24/09/2026 Philips BV Pulsera and Zenition Systems Medical Device Product Correction Class I Hospital
Official recall notice
Philips BV Pulsera and Zenition Systems
Agency: Therapeutic Goods Administration
Official publication date: September 24, 2026
Read the official AU_TGA_DRAC recall notice →SCAN ONCE. KEEP WATCHING.
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