FDA Device Intelligence
HomeDevice types › FSA

Lift, Patient, Non-Ac-Powered

FDA product code FSA · Class 1 · General Hospital

2,864
Registered devices
14,697
Adverse events
141
Recalls
13
510(k) clearances

Devices with this code

Recent 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 scenari
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 cust
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 cust
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 cust
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 cust
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
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

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.