FDA Device recall Z-1780-2022
Philips Respironics Amara View Minimal Contact Full-Face Mask
- FDA Device
- Class I
- ongoing
- Published 2022-10-12
On 2022-10-12 the FDA classified a Class I recall of Philips Respironics Amara View Minimal Contact Full-Face Mask by Philips Respironics, citing no contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1780-2022 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2022-09-06 |
| Published | 2022-10-12 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Philips Respironics |
| Distribution | US |
Product
Philips Respironics Amara View Minimal Contact Full-Face Mask
Reason
No contraindication/warning regarding magnetic components in CPAP masks for patients with implantable devices or metallic splinters in the eyes.
Identifiers
| code_info | All Units; Model No: 1090602, 1090603, 1090604, 1090622, 1090623, 1090624, 1090641, 1090642, 1090643, 1090644, 1090651,…All Units; Model No: 1090602, 1090603, 1090604, 1090622, 1090623, 1090624, 1090641, 1090642, 1090643, 1090644, 1090651, 1090652, 1090653, 1090654, 1090662, 1090663, 1090664, 1090670, 1090696, 1090697, 1135080, 1135081, 1135082, 1136626, 1090670RTL, 1136626RTL. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1780-2022%22
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