Stop using nowMedical device recall · FDA · Published August 14, 2026
Medline Basic Homecare Beds Fire Hazard: Pendant Overheating Risk
Medline recalls 771,127 Basic Homecare Beds due to fire risk from hand control pendant overheating. Affected beds may smoke, spark, melt or catch fire. Stop using immediately.
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.
“Medline Basic Homecare Beds Fire Hazard: Pendant Overheating Risk.” GovInfoNow, updated October 14, 2026. https://govinfonow.com/recall/1449359-medline-industries-lp-recalls-medline-basic-homecare-beds-and-medlite. Based on FDA recall #Z-3228-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3228-2026%22&limit=1).
The FDA announced on Aug. 14, 2026, that Medline Industries, LP is recalling Basic Homecare Beds and Medlite Homecare Beds due to a potential fire hazard from overheating hand control pendants. Owners should contact the company for a remedy.
How to tell if you have it
Brand: Medline
Product: Basic Homecare Beds
Product: Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
UDI-DI: 00080196288284
Lots: All lots
The hazard
The hand control pendant and associated wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. The recall includes additional products added to a Nov. 26, 2025, recall.
Context
GovInfoNow's records show Medline Industries, LP has 68 other recalls on record since July 31, 2025. Other recent recalls of similar products include Medline Convenience Kits Recall: Fungal Contamination Risk (Aug. 11, 2026), Medline Sinus Packs with Sharp Brush Edges Recalled for Cut Risk (Aug. 10, 2026), and Medline Industries, LP recalls Medline Convenience Kits (Aug. 10, 2026). Other recent recalls of similar products include Handy Solutions Neck & Should: Folded heating pad risks burns and fire (Feb. 18, 2026), CareFusion BD Pyxis MedBank Tower 1145-00: Fingerprint Scanner Overheats Risk (April 30, 2026), and BD Pyxis MedBank Mini 1147-00 Medication Cabinet Recall: Fingerprint Scanner Overheats Risk (April 30, 2026).
How to tell if you have this one
Look for the model MDR107000P with the part number UDI-DI 00080196288284. All lots of these beds are affected.
Brand
Medline
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Ongoing
Distribution
Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.
Recall number
Product, codes & lots
Z-3227-2026
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants: MDR510094 PENDANT F/ MDR107002E MDR520094 PENDANT F/ MDR107003E MDR530094 PENDANT, W/ 9V BATTERY BACKUP, F/ 2E BED MDR540094 PENDANT, W/ 9V BATTERY BACKUP, F/ 3E BED; MDR510094 UDI-DI 10888277363021 MDR520094 UDI-DI 10884389161692 MDR530094 UDI-DI 10197344119059 MDR540094 UDI-DI 10197344119066 All lots
Z-3228-2026
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE; MDR107000P UDI-DI 00080196288284 All lots
Based on the official FDA remedy
What to do — step by step
Stop using it now
Immediately stop using the affected bed as it poses a fire risk.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 54 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-3228-2026 (August 14, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3228-2026 to see it in context.
Plain-language summary written by qwen3:4b on October 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.