FDA Device recall Z-1011-2026
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E
- FDA Device
- Class I
- ongoing
- Published 2026-01-28
On 2026-01-28 the FDA classified a Class I recall of MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E by Medline Industries, citing medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its sp….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1011-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-11-26 |
| Published | 2026-01-28 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Medline Industries |
| Distribution | CA, PA |
Product
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4
Reason
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.
Identifiers
| code_info | 1) UDI/DI 40080196320999, All lots; 2) UDI/DI 40080196320999, All Lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1011-2026%22
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