Medline Homecare Beds and Hand Pendants
Hand pendants for Medline homecare beds can overheat, posing a fire hazard.
High risk
There is a reasonable chance that using it could cause serious health problems or death.
FDA Class I recall · How risk is rated
What happened
Medline Industries, LP recalled Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, including the MDR107000P BED and hand pendants, due to a potential fire hazard. The hand control pendant and associated wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. The recall began August 14, 2026, and was classified by the FDA on September 30, 2026.
Summary by Recall Canary from the FDA notice.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
2 products
Affected if its UDI-DI is listed.
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants
- UDI-DI
- 10888277363021
- 10884389161692
- 10197344119059
- 10197344119066
- Lot
- All lots
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, Manual, Medlite
- UDI-DI
- 00080196288284
- Lot
- All lots
Details
- Company began the recall
- Sold in
Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.
- Event ID
- 99827
- Recall numbers
- Z-3227-2026 to Z-3228-2026
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Device defect
Company began the recall
Classified by FDA
Added to FDA's Enforcement Report
Listed on Recall Canary
In FDA's weekly enforcement report
