Device recall: Craftmatic Model 1 Base for Dual Bed Configurations
Craftmatic Industries, Inc. (Pompano Beach, FL) initiated this device recall on 24 Mar 2017; FDA lists 2 product records under event 89765, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 93% of the 1,091 device enforcement events initiated in 2017 carry the same class.
Status: Ongoing. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Craftmatic Industries, Inc..
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Craftmatic Industries, Inc., Pompano Beach, FL.
Reason for recall
"A potential for dual-configured beds to separate or slip away from one another."
Distribution
"US Nationwide distribution - product was not distributed outside of the United States"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-1499-2022 | Craftmatic Model 1 Base for Dual Bed Configurations | N/A | Class II | Ongoing | 10 Aug 2022 |
| Z-1500-2022 | Legacy Base for Dual Bed Configurations | N/A | Class II | Ongoing | 10 Aug 2022 |
Context
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "A potential for dual-configured beds to separate or slip away from one another."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "US Nationwide distribution - product was not distributed outside of the United States"
Is the recall still ongoing?
FDA lists the status as Ongoing. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.