PIEPS DSP Pro, DSP Pro Ice, and DSP Sport Avalanche Transceivers
Summary
CPSC recall: PIEPS DSP Pro, DSP Pro Ice, and DSP Sport Avalanche Transceivers. By Pieps GMBH, of Austria. Hazard: The transceiver can switch modes unexpectedly when not locked or installed in the harness. When this occurs, it will prevent the transceiver from transmitting a signal and can make it difficult to locate a skier in an avalanche, which can result in severe bodily harm or death.. Remedy: Consumers should immediately stop using the recalled avalanche transceivers and contact Black Diamo
Details
Source
CPSC Consumer Product Recall
External ID
9036
Action Date
2021-04-12
Status
Recalled
Category
consumer_product
Product Description
This recall involves all PIEPS DSP Pro, DSP Pro Ice, and DSP Sport Avalanche Transceivers. The transceivers are worn by
Company
Context & Analysis
This is a unclassified recall.
This was one of 7 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Pieps GMBH, of Austria 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 (Pieps GMBH, of Austria) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pieps GMBH, of Austria have FDA actions?
Pieps GMBH, of Austria 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 "9036" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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