FDA Device recall Z-1499-2022
Craftmatic Model 1 Base for Dual Bed Configurations
- FDA Device
- Class II
- ongoing
- Published 2022-08-10
On 2022-08-10 the FDA classified a Class II recall of Craftmatic Model 1 Base for Dual Bed Configurations by Craftmatic Industries, citing A potential for dual-configured beds to separate or slip away from one another.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1499-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-03-24 |
| Published | 2022-08-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Craftmatic Industries |
| Distribution | US |
Product
Craftmatic Model 1 Base for Dual Bed Configurations
Reason
A potential for dual-configured beds to separate or slip away from one another.
Identifiers
| code_info | 4AM663, 4AM669, 4AR391, 4AR445, 4AR797, 4AR790, 4AR795 |
|---|
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-1499-2022%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.