Invacare PerfectO2 Oxygen Concentrator Capacitor Recall for Fire Hazard
Invacare is recalling Dianz Capacitors used in PerfectO2 Oxygen Concentrators because they may rupture and cause a fire.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall involves a potential fire hazard, which constitutes a significant injury risk, aligning with the 'Severe' criteria for significant injury reports or high-risk defects.
Plain-English summary
Invacare Corporation is recalling a specific component, the Dianz Capacitor, which is used in the PerfectO2 Oxygen Concentrator. The recall is being conducted because the firm has identified that the capacitor has ruptured, creating a potential fire hazard.
The affected product was distributed throughout the United States and to foreign countries, including Canada and other unspecified locations. The distribution also included eight government consignees. A total of 138,446 units were distributed globally.
Consumers should check their devices for the specific serial numbers listed in the official recall documentation to determine if they are affected. If a device is found to be affected, users should follow the instructions provided by Invacare Corporation to address the fire risk.
The recalled product
- Product
- Component- Dianz Capacitor used in PerfectO2 Oxygen Concentrator, packaged one unit per box.
- Manufacturer
- Invacare Corporation
- Hazard
- Affected units
- 138,446
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- The following serial numbers are affected by this recall: (Also
Distribution
Distribution scope not specified by the agency.
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