Severity
Moderate
Zhongshan Lebo Medical Co., Ltd., of China issued this CPSC recall on January 8, 2026. Classified as Moderate severity. Approximately About 5,000 units are affected. The recall was issued because: The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attac…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.
This CPSC action (record #26165) was formally reported on January 8, 2026. It is classified under Moderate severity, with a current status of Active. Zhongshan Lebo Medical Co., Ltd., of China is listed as the recalling firm. Federal records indicate About 5,000 units are affected.
The documented reason for this recall is: The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of… Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: Consumers should immediately stop using the recalled adult portable bed rails and contact Agrish Direct for a full refund. Consumers should go to http://www.agrish.online/recall to register for the r… — consumers holding this product should act on that instruction rather than relying on general guidance.
To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by CPSC. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. Because this recall is recent, remedy windows and replacement inventory are most likely still actively available from the firm or retailer. Always cross-check the recall number against the official agency page before relying on any summary.
Severity
Moderate
Units Affected
About 5,000
Related Recalls
6
6 from same agency
This recall involves Agrish-branded adult portable bed rails, models 2512, 2513, and 2516, for use on adult beds. The model numbers are printed in the owner's manual. The recalled bed rails have white tubing with rounded gray foam rubber handle grips. Some models include a gray fabric pouch, support legs and a motion-sensor light. Recalled Bed Rails: Model Numbers Size zip 2512 About 11 inches wide and 39 inches in height About 12 inches wide and 42 inches in height 2516 About 37 inches wide and 45 inches in height
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation.
Consumers should immediately stop using the recalled adult portable bed rails and contact Agrish Direct for a full refund. Consumers should go to http://www.agrish.online/recall to register for the recall and receive instructions on how to dispose of the recalled bed rail.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 26165 |
| Date reported | January 8, 2026 |
| Date initiated | January 8, 2026 |
| Recalling firm | Zhongshan Lebo Medical Co., Ltd., of China |
| Units affected | About 5,000 |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
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Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.
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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).