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Proactive

XIAMEN WORLD GEAR SPORTS GOODS CO., LTD · Model 32475 · UDI-DI 06974512010014

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

Description

The Proactive Medical patient lift is intended to transfer an individual from one resting surface to another (such as a bed to a wheelchair).

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.