Z-1013-2026Class I

MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare...

Name: Z-1013-2026 MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare...
Creator: Medline Industries, LP
Published: 2025-11-26
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2025-11-26 / Open, Classified / root cause: design

FDA source

Medline Industries, LP began a recall of MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4 on 2025-11-26. FDA classified it as Class I and gives the reason as "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...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as design.

Recall record

Recall number: Z-1013-2026
Classification: Class I
Status: Open, Classified
Initiated: 2025-11-26
Posted: 2026-01-16
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.
Product code: LLI Bed, Therapeutic, Ac-Powered, Adjustable Home-Use
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.
Root cause tag: design
FDA root cause: Device Design
Action: Medline issued an URGENT MEDICAL DEVICE RECALL notice with an enclosed URGENT MEDICAL DEVICE FIELD CORRECTION NOTICE to its consignees on 11/26/2025 via email and USPS first class mail. The notice explained the issue, potential risks, and requested the user ONLY USE MEDLINE SIDE RAILS and MEDLINE ACCESSORIES that are intended for use with Medline Homecare Beds. When using Medline Side Rails and Medline Accessories, follow all applicable instructions for use. Distributors were directed to notify their customers. For questions, contact the Recall Department at 866-359-1704 [email protected].
Quantity in commerce: 138412 units
Distribution: US, CA, PA, GUAM, VI
Product codes and lots: 1) REF MDR107003E, UDI/DI 40080196321002, All lots; 2) REF MDR107003E-4, UDI/DI 40080196321002, All lots

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1013-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1011-2026	Class I	Ongoing	Voluntary: Firm initiated	2026-01-28	2026-01-16
Z-1012-2026	Class I	Ongoing	Voluntary: Firm initiated	2026-01-28	2026-01-16
Z-1013-2026	Class I	Ongoing	Voluntary: Firm initiated	2026-01-28	2026-01-16
Z-1014-2026	Class I	Ongoing	Voluntary: Firm initiated	2026-01-28	2026-01-16
Z-1015-2026	Class I	Ongoing	Voluntary: Firm initiated	2026-01-28	2026-01-16
Z-1016-2026	Class I	Ongoing	Voluntary: Firm initiated	2026-01-28	2026-01-16

Product code LLI

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)