CLASS II ONGOING Device recall · Reported 10 Aug 2022 · FDA Enforcement Report
Legacy Base for Dual Bed Configurations recalled
Craftmatic Industries is recalling Legacy Base for Dual Bed Configurations, distributed nationwide in the US. The recall was initiated on 24 Mar 2017 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1500-2022
- FDA event ID
- 89765
- Recalling firm
- Craftmatic Industries, Pompano Beach, FL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 24 Mar 2017
- FDA classified
- 4 Aug 2022
- Reported
- 10 Aug 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 24 Mar 2017 | Recall initiated by company | |
| 4 Aug 2022 | Classified by FDA | +1959 days |
| 10 Aug 2022 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
A potential for dual-configured beds to separate or slip away from one another.
Product as listed by the FDA
Legacy Base for Dual Bed Configurations
Where it was distributed
US Nationwide distribution - product was not distributed outside of the United States
Questions about this recall
Why was it recalled?
A potential for dual-configured beds to separate or slip away from one another.
Which lots are affected?
4AT056, 4AT061, 4AT063
Where was it sold?
US Nationwide distribution - product was not distributed outside of the United States
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 89765This product is part of a recall event; the main page for the event is Craftmatic Model 1 Base for Dual Bed Configurations recalled.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | Craftmatic Model 1 Base for Dual Bed Configurations recalled | Craftmatic Industries | Other | Nationwide |
More recalls from Craftmatic Industries
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Craftmatic Model 1 Base for Dual Bed Configurations recalled | Craftmatic Industries | Other | Nationwide |
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