Recall Z-1499-2022— Craftmatic Industries, Inc.
Class II · Ongoing
Class II FDA medical device recall by Craftmatic Industries, Inc., initiated 2017-03-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Craftmatic Model 1 Base for Dual Bed Configurations. Reason: A potential for dual-configured beds to separate or slip away from one another..
- Recalling firm
- Craftmatic Industries, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2017-03-24
- Firm location
- Pompano Beach, FL, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.