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Vancare Vanderlift
VANCARE INC · Model Vanderlift II EB450 · UDI-DI 00850030758149
10
510(k) clearances
15,182
Adverse events (428 deaths)
141
Recalls
206
Facilities
Description
Full body mobile floor lift with electric base option. Weight capacity 450 lbs. Purple in color.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-10 | ARJOHUNTLEIGH POLSKA Sp. z.o.o. | An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss |
| 2025-12-18 | Community Products, LLC | Potential for fraying on the body support strap. |
| 2025-12-18 | Community Products, LLC | Potential for fraying on the body support strap. |
| 2025-12-18 | Community Products, LLC | Potential for fraying on the body support strap. |
| 2025-11-17 | ETAC A/S | A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it b |
| 2025-11-17 | ETAC A/S | A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it b |
| 2025-11-17 | ETAC A/S | A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it b |
| 2025-11-17 | ETAC A/S | A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it b |
| 2025-05-30 | Baxter Healthcare Corporation | The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury fro |
| 2025-05-30 | Baxter Healthcare Corporation | The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury fro |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.