OFFICIAL-SOURCE RECALL · CANADA
FreeO2 Automated Oxygen Therapy Device Adult & Pediatric - Version Recall: Under specific conditions
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
- FreeO2 Automated Oxygen Therapy Device Adult & Pediatric - Version HW 2.3
- 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
Under specific conditions following a deep battery discharge, error 29515 may occur during startup of a FreeO2 HW 2.3 device using software package 1.4.2 and prevent its use. The update to software package 1.4.3 corrects this issue and restores the expected startup behaviour.
Hazard
Under specific conditions following a deep battery discharge, error 29515 may occur during startup of a FreeO2 HW 2.3 device using software package 1.4.2 and prevent its use. The update to software package 1.4.3 corrects this issue and restores the expected startup behaviour.
Official recall notice
FreeO2 Automated Oxygen Therapy Device Adult & Pediatric - Version HW 2.3
Agency: Health Canada
Official publication date: October 8, 2026
Read the official CANADA_MEDICAL_DEVICES recall notice →SCAN ONCE. KEEP WATCHING.
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