MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed — Class I medical device recall Z-1011-2026
Ongoing recall by Medline Industries, LP, reported 2026-01-28, distributed in CA, GU, PA. Medline Industries has identified a potential hazard involving the hand control pendant and associated wires.
| Recall number | Z-1011-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-11-26 |
| Classified | 2026-01-16 |
| Reported by FDA | 2026-01-28 |
| Distributed | CA, GU, PA |
| Quantity | 373,392 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 40080196320999 |
| Model numbers | MDR107002E, MDR107002E-4 |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1011-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.