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Cirrus Ceiling Lift - Tollos

1073849 Ontario Limited · Model 00817956021269 · UDI-DI 00817956021269

FSA
10
510(k) clearances
15,182
Adverse events (428 deaths)
142
Recalls
205
Facilities

Description

750 lbs Capacity Cloth belt Old Tollos Track Series (T6010 and T6015) Quick Release Docking Charge Standard hand controller 6-point spreader bar

Recalls

DateFirmReason
2026-09-14Baxter Healthcare CorporationPotential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift strap lowers more quic
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

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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.