Beal Birdie Belay Devices
Summary
CPSC recall: Beal Birdie Belay Devices. By Beal Sas, of France. Hazard: The device user can be unable to lower the climber, posing a risk of injury to the climber.. Remedy: Consumers should immediately stop using the recalled Beal Birdie Belay Devices and contact Liberty Mountain for a free replacement..
Details
Source
CPSC Consumer Product Recall
External ID
9024
Action Date
2021-03-24
Status
Recalled
Category
consumer_product
Product Description
The Beal Birdie Belay Device is used by rock climbers. Belay devices are used with climbing ropes to protect the climber
Company
Context & Analysis
This is a unclassified recall.
This was one of 8 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Beal Sas, of France has 2 FDA actions in our database, including 1 recall.
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 (Beal Sas, of France) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Beal Sas, of France have FDA actions?
Beal Sas, of France has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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