CLASS I ONGOING Device recall · Reported 28 Jan 2026 · FDA Enforcement Report
Medline beds labeled as: Full Electric Lightweight Homecare Bed recalled
Medline Industries is recalling Medline beds labeled as: Full Electric Lightweight Homecare Bed, distributed in California, Pennsylvania. The recall was initiated on 26 Nov 2025 and the FDA has classified it as Class I.
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-1015-2026
- FDA event ID
- 98185
- Recalling firm
- Medline Industries, Northfield, IL
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 26 Nov 2025
- FDA classified
- 16 Jan 2026
- Reported
- 28 Jan 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Other Medical Devices
Timeline
| 26 Nov 2025 | Recall initiated by company | |
| 16 Jan 2026 | Classified by FDA | +51 days |
| 28 Jan 2026 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
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.
Product as listed by the FDA
MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
Where it was distributed
US, CA, PA, GUAM, VI
Questions about this recall
Why was it recalled?
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.
Which lots are affected?
UDI/DI 40080196294344, All lots
Where was it sold?
US, CA, PA, GUAM, VI
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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
5 other products · FDA event 98185| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | Medline beds labeled as: Full Electric Low Basic Homecare Bed recalled | Medline Industries | Other | CA, PA | |
| CLASS I | Medline beds labeled as: Full Electric Basic Homecare Bed recalled | Medline Industries | Other | CA, PA | |
| CLASS I | Medline beds labeled as: Full Electric Low Lightweight Homecare Bed recalled | Medline Industries | Other | CA, PA | |
| CLASS I | Medline beds labeled as: Semi Electric Lightweight Homecare Bed recalled | Medline Industries | Other | CA, PA | |
| CLASS I | Medline beds labeled as: Semi Electric Basic Homecare Bed recalled | Medline Industries | Other | CA, PA |
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