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Vancare Vanderlift

VANCARE INC · Model Vanderlift 450 - White · UDI-DI 00850030758019

FSA
10
510(k) clearances
14,697
Adverse events (423 deaths)
141
Recalls
206
Facilities

Description

Full Body patient mobile floor lift. 450 lb weight capacity. White in color.

Recalls

DateFirmReason
2026-03-10ARJOHUNTLEIGH 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
2025-12-18Community Products, LLCPotential for fraying on the body support strap.
2025-12-18Community Products, LLCPotential for fraying on the body support strap.
2025-12-18Community Products, LLCPotential for fraying on the body support strap.
2025-11-17ETAC A/SA 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
2025-11-17ETAC A/SA 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
2025-11-17ETAC A/SA 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
2025-11-17ETAC A/SA 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
2025-05-30Baxter Healthcare CorporationThe 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
2025-05-30Baxter Healthcare CorporationThe 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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Data 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.