Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE was recalled because potential risk of fire involving the hand control pendant and associated wiring used with affected beds. pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. additional products added to 11/26/2025 recall.. If you have this product, stop using it until you verify your lot or model details.
By RecallRadar Editorial Team
Sourced from FDA. Last verified October 13, 2026.
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Check if you qualifyKey facts
- Date announced
- October 7, 2026
- Source agency
- FDA
This recall involves safety concerns. Take action promptly.
✨ Plain-English Summary
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE was recalled because potential risk of fire involving the hand control pendant and associated wiring used with affected beds. pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. additional products added to 11/26/2025 recall.. If you have this product, stop using it until you verify your lot or model details.
Is This Recall Still Active?
Status: Yes - Active
This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.
What's Being Recalled
Quoted source excerpt from the official notice.
Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.
Quick Info
Key facts from the official notice, kept in the article flow for easy cross-checking.
- Brand
- Medline industries, lp
- Category
- medical
- Source agency
- FDA
- Announced
- October 7, 2026
- Country
- US
- Status
- Active
Who's Affected
Specific models and identifiers listed in the source notice:
Model #1
MDR107000P UDI-DI 00080196288284 All lots
| # | Model |
|---|---|
| 1 | MDR107000P UDI-DI 00080196288284 All lots |
Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.
What You Should Do
Follow the remedy path from the official notice using the exact model and serial details above.
- 1Stop using the affected product until you verify whether your item is impacted.
- 2Check the official recall notice and match your model, lot, or serial details.
- 3Follow the official instructions for repair, replacement, refund, or disposal.
Source & Verification
This page summarizes the official notice and keeps key facts easy to verify.
- Official source
- FDA
- Announced by source
- October 7, 2026
- Last reviewed by RecallRadar
- October 13, 2026
Frequently Asked Questions
Am I affected by this recall?
Check the affected models section on this page. The official notice currently lists MDR107000P UDI-DI 00080196288284 All lots.
What is the remedy for this recall?
Follow the official instructions for repair, replacement, refund, or disposal on the medline industries, lp recall page.
Where can I verify recall details?
Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/device/enforcement.json?search=recall_number:Z-3228-2026&limit=1
Keep browsing with these internal hubs: medline industries, lp recall hub and Medical recall hub.
Official Resources
Use these primary sources for final eligibility and claim instructions.
View official notice from FDASee an inaccuracy?
Help us improve the accuracy of this recall information.
On this page
Free checker
Check if you qualify
See whether your device may qualify for a free repair or replacement program before you spend money.
Check if you qualifyKey facts
- Date announced
- October 7, 2026
- Source agency
- FDA
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