Medline Industries, LP medical device recall: MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Medical devices
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 98185
- Recall initiated
- Nov 26, 2025
- Classified by FDA
- Jan 16, 2026
- Posted in Enforcement Report
- Jan 28, 2026
- Recalling firm
- Medline Industries, LP
- Firm location
- Northfield, IL, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Letter
- Products in this event
- 6
What to do
Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.
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.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Nov 26, 2025. FDA classified it 51 days later, on Jan 16, 2026. This recall event covers 6 separate products, each with its own FDA recall number. Distribution reported by FDA: US, CA, PA, GUAM, VI Medline Industries, LP has 257 recalls in our records.
Recalled products (6)
Z-1011-2026 Class I Ongoing
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4
Codes / lots: 1) UDI/DI 40080196320999, All lots; 2) UDI/DI 40080196320999, All Lots
Quantity: 373392 units
Z-1012-2026 Class I Ongoing
MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
Codes / lots: UDI/DI 40080196294320, All lots
Quantity: 13245 units
Z-1013-2026 Class I Ongoing
MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.
Codes / lots: 1) REF MDR107003E, UDI/DI 40080196321002, All lots; 2) REF MDR107003E-4, UDI/DI 40080196321002, All lots
Quantity: 138412 units
Z-1014-2026 Class I Ongoing
MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
Codes / lots: UDI/DI 10080196546992, All lots
Quantity: 22565 units
Z-1015-2026 Class I Ongoing
MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
Codes / lots: UDI/DI 40080196294344, All lots
Quantity: 35694 units
Z-1016-2026 Class I Ongoing
MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
Codes / lots: UDI/DI 40080196325901, All lots
Quantity: 15581 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA device enforcement dataset
- Official notice
- FDA Enforcement Report, event 98185
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.