Humanscale Recalls QuickStand Lite Workstations Due to Injury Hazard
Reported: September 17, 2019 Initiated: September 17, 2019 #19205
Product Description
This recall involves QuickStand Lite height adjustable workstations for single or double computer monitor screens. The workstations have a keyboard platform and an adjustable arm. The workstations measure about 19.5 inches high and about 25.6 inches wide. The workstations were sold in black and white with gray trim.
Reason for Recall
The recalled workstation's arm can break and cause the workstation to fall, posing a risk of injury.
Remedy
Consumers should immediately stop using the recalled workstation and contact Humanscale to receive a free repair kit.
Details
- Units Affected
- About 22,700 (In addition, about 2,200 were sold in Canada)
Frequently Asked Questions
What product was recalled? ▼
This recall involves QuickStand Lite height adjustable workstations for single or double computer monitor screens. The workstations have a keyboard platform and an adjustable arm. The workstations measure about 19.5 inches high and about 25.6 inches wide. The workstations were sold in black and white with gray trim.. Units affected: About 22,700 (In addition, about 2,200 were sold in Canada).
Why was this product recalled? ▼
The recalled workstation's arm can break and cause the workstation to fall, posing a risk of injury.
What should consumers do? ▼
Consumers should immediately stop using the recalled workstation and contact Humanscale to receive a free repair kit.
Which agency issued this recall? ▼
This recall was issued by the CPSC on September 17, 2019. Severity: Moderate. Recall number: 19205.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11