Rhino 24-foot Hot Foot Climbing Sticks
Summary
CPSC recall: Rhino 24-foot Hot Foot Climbing Sticks. By Amazon.com, Walmart.com and other sporting goods stores nationwide from January 2021 through December 2023 for about $100.. Hazard: The climbing sticks can break at the weld point, posing fall and laceration hazards to consumers.. Remedy: Consumers should immediately stop using the recalled climbing sticks and contact FeraDyne to receive a full refund. Consumers can return the recalled product with a FeraDyne-provided prepaid mailer or rece
Details
Source
CPSC Consumer Product Recall
External ID
9855
Action Date
2024-02-15
Status
Recalled
Category
consumer_product
Product Description
This recall involves Rhino branded 24-foot Hot Foot Climbing Sticks used in game hunting. They have extended tree braces
Context & Analysis
This is a unclassified recall.
This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
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 (Amazon.com, Walmart.com and other sporting goods stores nationwide from January 2021 through December 2023 for about $100.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Amazon.com, Walmart.com and other sporting goods stores nationwide from January 2021 through December 2023 for about $100. have FDA actions?
This is the only FDA action we have on record for Amazon.com, Walmart.com and other sporting goods stores nationwide from January 2021 through December 2023 for about $100. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9855" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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