Data Foundry

Medical device recalls 2022

Legacy Base for Dual Bed Configurations — Class II medical device recall Z-1500-2022

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 numberZ-1500-2022
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCraftmatic Industries, Inc., Pompano Beach, FL, United States
Recall initiated2017-03-24
Classified2022-08-04
Reported by FDA2022-08-10
DistributedNationwide (US)

Product

Legacy 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-1500-2022. 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.