[Recalled] Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model) — Between March 2, 2021 and December 31, 2021, the product label used in producti… | FDA 2022-06-10
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model) |
|---|---|
| Brand / manufacturer | Invacare Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1369-2022 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 10 June 2022 |
| EAN / barcode | 00841447112075 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Between March 2, 2021 and December 31, 2021, the product label used in production did not contain the "Rx Only" statement as required.
This Class III recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Invacare Corporation
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.