Nimbus Lock Carabiners
The firm has received 21 reports of the closing mechanism breaking. No injuries have been reported.
Summary
CPSC recall: Nimbus Lock Carabiners. By The firm has received 21 reports of the closing mechanism breaking. No injuries have been reported.. Hazard: The carabiner's automatic closing mechanism can break and prevent the gate from closing, posing a risk of serious injury or death due to falling.. Remedy: Consumers should immediately stop using the recalled Nimbus Lock Carabiners and contact C.A.M.P. Consumers will be asked to fill out the recall form at www.camp-usa.com/nimbus-lock-safety-recall-r
Details
Source
CPSC Consumer Product Recall
External ID
10389
Action Date
2025-08-28
Status
Recalled
Category
consumer_product
Product Description
This recall involves Nimbus Lock Carabiners sold in Gun Metal/Green, Gun Metal/Fuchsia and Gun Metal/Blue. The affected
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.
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 (The firm has received 21 reports of the closing mechanism breaking. No injuries have been reported.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The firm has received 21 reports of the closing mechanism breaking. No injuries have been reported. have FDA actions?
This is the only FDA action we have on record for The firm has received 21 reports of the closing mechanism breaking. No injuries have been reported. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10389" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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