Craftmatic Model 1 Base for Dual Bed Configurations — Class II medical device recall Z-1499-2022
Ongoing recall by Craftmatic Industries, Inc., reported 2022-08-10, distributed nationwide. A potential for dual-configured beds to separate or slip away from one another.
| Recall number | Z-1499-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Craftmatic Industries, Inc., Pompano Beach, FL, United States |
| Recall initiated | 2017-03-24 |
| Classified | 2022-08-04 |
| Reported by FDA | 2022-08-10 |
| Distributed | Nationwide (US) |
Product
Craftmatic Model 1 Base for Dual Bed Configurations
Reason for recall
A potential for dual-configured beds to separate or slip away from one another.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1499-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.