FDA Device recall Z-3228-2026
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
- FDA Device
- Class I
- ongoing
- Published 2026-10-07
On 2026-10-07 the FDA classified a Class I recall of Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE by Medline Industries, citing 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, spa….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3228-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-08-14 |
| Published | 2026-10-07 |
| Last updated | 2026-10-13 05:30 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
Reason
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.
Identifiers
| code_info | MDR107000P UDI-DI 00080196288284 All lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-10-13 05:30 UTC. Current status: ongoing.
Other recalls by Medline Industries
- Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories, Hand Pendants: MDR510094 PENDANT F/ MDR107002E MDR520094 PENDANT F/…
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3228-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.