KLIM Backcountry Probes A300
Summary
CPSC recall: KLIM Backcountry Probes A300. By Online at www.klim.com and at KLIM and Polaris dealers nationwide from October 2022 through November 2022 for about $80.. Hazard: The recalled probes can fail to operate when deployed by rescuers, posing a risk of severe injury or death to a person buried under snow following an avalanche.. Remedy: Consumers should immediately stop using the recalled probes and contact KLIM by email at orders@KLIM.com and enter "A300 Probe Recall" in the subject line
Details
Source
CPSC Consumer Product Recall
External ID
9532
Action Date
2023-02-16
Status
Recalled
Category
consumer_product
Product Description
This recall involves KLIM Backcountry Probes A300, which are used to locate people buried in snow following an avalanche
Context & Analysis
This is a unclassified recall.
This was one of 15 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 (Online at www.klim.com and at KLIM and Polaris dealers nationwide from October 2022 through November 2022 for about $80.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Online at www.klim.com and at KLIM and Polaris dealers nationwide from October 2022 through November 2022 for about $80. have FDA actions?
This is the only FDA action we have on record for Online at www.klim.com and at KLIM and Polaris dealers nationwide from October 2022 through November 2022 for about $80. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9532" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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