Device recall
Z-1015-2026: MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
FDA device recall · Class I · Medline Industries, LP
Key facts
| Recall number (Z-number) | Z-1015-2026 |
|---|---|
| Recall event | 98185 |
| Product | MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L |
| Product code | LLI |
| Recalling firm | Medline Industries, LP |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1417592 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database