TRUBLUE iQ Auto Belay Devices
Summary
CPSC recall: TRUBLUE iQ Auto Belay Devices. By Head Rush Technologies, of Louisville, Colorado. Hazard: The recalled auto belay device can fail to retract, posing a fall hazard and risk of serious injury or death.. Remedy: Consumers should immediately stop using recalled auto belay devices, and contact Head Rush Technologies for a free inspection and repair..
Details
Source
CPSC Consumer Product Recall
External ID
9983
Action Date
2024-06-20
Status
Recalled
Category
consumer_product
Product Description
This recall involves TRUBLUE iQ Auto Belay Devices, which enable climbers to safely descend while climbing. The TRUBLUE
Context & Analysis
This is a unclassified recall.
This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Head Rush Technologies, of Louisville, Colorado has 6 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Head Rush Technologies, of Louisville, Colorado) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Head Rush Technologies, of Louisville, Colorado have FDA actions?
Head Rush Technologies, of Louisville, Colorado has 6 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9983" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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