FDA Device recall Z-0918-2022
Cub 2 Enclosed Bed Canopy System
- FDA Device
- Class I
- ongoing
- Published 2022-04-20
On 2022-04-20 the FDA classified a Class I recall of Cub 2 Enclosed Bed Canopy System by Sensory Medical, citing due potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0918-2022 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2022-03-14 |
| Published | 2022-04-20 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Sensory Medical |
| Distribution | US |
Product
Cub 2 Enclosed Bed Canopy System
Reason
Due potential misuse of the product, firm is updating warnings and precautions booklet for products distributed before December 16, 2021.
Identifiers
| code_info | Model/Product Code - Cub2 UDI Code: None Serial Numbers: All device manufactured/distributed prior to 12/16/2021. |
|---|
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-0918-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.