Liberty Mountain Recalls Singing Rock Climbing Lanyards Due to Injury Risk
Liberty Mountain is recalling Singing Rock Easy Go XP Lock Via Ferrata Lanyards because the elastic webbing can break, posing a risk of serious injury or death.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product where the hazard is serious injury or death, but no injuries have been reported, which aligns with the 'High' severity criteria.
Plain-English summary
Liberty Mountain, of Salt Lake City, Utah, is recalling approximately 140 Singing Rock Easy Go XP Lock Via Ferrata Lanyards. These products are used for shock absorption on Via Ferrata mountain climbing routes and feature two elasticized webbing branches with self-locking carabiners at each end. The recalled units can be identified by the elasticized webbing and a white tag sewn into the zipper pouch that reads "EASY GO XP LOCK."
The recall was issued because the elastic webbing on the lanyards can deteriorate over time and break while in use. This failure poses a risk of serious injury or death to the climber. No injuries have been reported in connection with this recall.
The lanyards were sold at specialty climbing shops nationwide and online at Amazon.com and other internet retailers between April 2011 and August 2012 for about $120. Consumers should immediately stop using the recalled lanyards and contact Liberty Mountain for a refund or replacement. Liberty Mountain can be reached toll-free at (800) 366-2666 from 8 a.m. to 5 p.m. MT Monday through Friday, or online at www.libertymountain.com.
The recalled product
- Product
- Easy Go XP Lock Via Ferrata Lanyards
- Manufacturer
- Singing Rock, of Ponikla, Czech Republic
- Category
- Consumer Product — Climbing Gear
- Affected units
- 140
Distribution
Distributed nationwide across the United States.
Related recalls
Same hazard · equipment failure
See all →- HighGE Optima XR200/220/240amx Radiographic System Column Safety Mechanism
FDA (Devices) · 2026-07-22
- HighMobile Digital Radiographic System Arm Drop Risk During Patient Exams
FDA (Devices) · 2026-07-22
- SevereCyberknife Treatment Delivery System Collimator Docking and Fall Hazard Recall
FDA (Devices) · 2026-07-08
- SevereOmnipod Eros Pod Insulin Delivery Failure Risk
FDA (Devices) · 2026-07-08
- HighPetzl America Recalls Three Climbing Harness Models for Fall Hazard
CPSC · 2026-05-14