FDA Device recall Z-0148-2023
sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin
- FDA Device
- Class II
- terminated
- Published 2022-11-09
On 2022-11-09 the FDA classified a Class II recall of sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin by Sentec Ag, citing weak skin adhesion.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0148-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-08-22 |
| Published | 2022-11-09 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Sentec Ag |
| Distribution | US |
Product
sentec 24 / MARe-SF Multi-Site Attachment Ring Easy, For sensitive / fragile skin. Used in continuous, noninvasive carbon dioxide and/or oxygen tension monitoring.
Reason
Weak skin adhesion.
Identifiers
| code_info | batch #220139 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0148-2023%22
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