RecallHawk

PIEPS DSP Pro, DSP Pro Ice, and DSP Sport Avalanche Transceivers

Pieps GMBH, of Austria

Summary

CPSC recalled 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 Diamond for a free replacement hardcase carrying system and user guide to be used with the recalled transceivers..

Details

Source

cpsc

External ID

21108

Action Date

2021-04-12

Status

Ongoing

Category

product

Product Description

This recall involves all PIEPS DSP Pro, DSP Pro Ice, and DSP Sport Avalanche Transceivers. The transceivers are worn by skiers so they can be located if they are buried in an avalanche. The units were sold in one size with an LCD display, a slider switch with Off/Search/Send, and are powered by a battery. The devices have a green/yellow, black/yellow, or clear/yellow exterior. The transceivers come with a black neoprene carrying case. The manufacturer's name, PIEPS, is printed in black letters on the front of the unit with the model name DSP Pro, DSP Pro Ice, and DSP Sport. The recall includes PIEPS DSP Sport Avalanche Transceiver MODEL NO. PP1128040000ALL1; PIEPS DSP Pro Avalanche Transceiver MODEL NO. PP1127710000ALL1; and PIEPS DSP Pro Ice Avalanche Transceiver MODEL NO. PP1127700000ALL1. The model name DSP02 can be found on the inside of the battery door, and the model number can be found on the outside of the packaging.

Context & Analysis

Pieps GMBH, of Austria has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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