FDA Device recall Z-1783-2022
Wisp and Wisp Youth Nasal Mask
- FDA Device
- Class I
- ongoing
- Published 2022-10-12
On 2022-10-12 the FDA classified a Class I recall of Wisp and Wisp Youth Nasal 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-1783-2022 |
| 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
Wisp and Wisp Youth Nasal 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.: 1094050, 1094051, 1094053, 1094060, 1094061, 1094062, 1094070, 1094071, 1094072, 1094073, 1109298…All Units; Model No.: 1094050, 1094051, 1094053, 1094060, 1094061, 1094062, 1094070, 1094071, 1094072, 1094073, 1109298, 1113954, 1117119, 1118060, 1118061, 1118062, 1118063, 1118064, 1118065, 1118066, 1118067, 1120434, 1137360, 1137361, 1137366, 1137367, 1137368, 1137369, 1137370, 1138989, 1138991, 1138992, 1138993, 1138994, 1138995, 1138996, 1139009, 1148366, 1094051RTL. |
|---|
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-1783-2022%22
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