- Recalling firm
- Medline Industries, LP
- 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.
- Affected products (lot / model / serial)
- MDR510094 UDI-DI 10888277363021 MDR520094 UDI-DI 10884389161692 MDR530094 UDI-DI 10197344119059 MDR540094 UDI-DI 10197344119066 All lots
- Units affected
- 771,127 total
- Distribution pattern
- Distribution US Nationwide including territories of Puerto Rico and Guam and the countries of Bermuda, Canada, and Panama.
- Firm location
- Northfield, IL, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-3227-2026
- Recall initiated
- August 14, 2026
- FDA classification date
- September 30, 2026
- FDA report date
- October 7, 2026
- FDA event ID
- 99827
- Last updated on HTM Vibe
- October 13, 2026
