RecallRadar
FDA · Medical devicesClass I

Medline Industries, LP medical device recall: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Medical devices
Classification
Class I
Status
Ongoing
Event ID
99827
Recall initiated
Aug 14, 2026
Classified by FDA
Sep 30, 2026
Posted in Enforcement Report
Oct 7, 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
2

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.

View the official FDA record ↗

Reason for recall

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.

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 Aug 14, 2026. FDA classified it 47 days later, on Sep 30, 2026. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama. Medline Industries, LP has 257 recalls in our records.

Recalled products (2)

  • Z-3227-2026 Class I Ongoing

    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

    Codes / lots: MDR510094 UDI-DI 10888277363021 MDR520094 UDI-DI 10884389161692 MDR530094 UDI-DI 10197344119059 MDR540094 UDI-DI 10197344119066 All lots

    Quantity: 771,127 total

  • Z-3228-2026 Class I Ongoing

    Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE

    Codes / lots: MDR107000P UDI-DI 00080196288284 All lots

    Quantity: 771,127 total

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 99827
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.

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