Fresh Recalls

FDAClass I · Medical device · Recall Z-3228-2026 · Recalled October 7, 2026

Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED recall — Medline Industries, LP

Agency report date: October 7, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED
Company / brand
Medline Industries
Lot / serial / date codes
MDR107000P UDI-DI 00080196288284 All lots
Distribution
Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED recall status

3. Open the official notice or contact

Official recall ID
Z-3228-2026
Brand
All Medline Industries recalls
Classification
Class I
Units affected
771,127 total
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Northfield, IL, United States
Firm address
3 Lakes Dr, 60093-2753

Identifying details (verbatim from the notice)

Product codes / lots
MDR107000P UDI-DI 00080196288284 All lots
Distribution
Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.
Firm notified the public via
Letter
FDA event ID
99827
Recall initiated
August 14, 2026
FDA classified
September 30, 2026
FDA report date
October 7, 2026

More Medline Industries recalls

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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