RecallHawk

Avalanche Transceivers

Unknown Manufacturer

Summary

CPSC recalled Avalanche Transceivers by Unknown Manufacturer. Hazard: The recalled transceivers may not switch from SEND mode into SEARCH mode. If this were to occur, the device would not be able to locate a skier in an avalanche, which could result in severe bodily harm or death if the skier is buried under snow.. Remedy: Consumers should immediately stop using the recalled transceivers and perform a safety check to verify if the device can switch into Search Mode by following instructions on this website. If the devices are not working properly, please contact Black Diamond to receive a prepaid shipping label to return the recalled transceivers for a free repair or a replacement device..

Details

Source

cpsc

External ID

22194

Action Date

2022-07-28

Status

Ongoing

Category

product

Product Description

This recall involves the PIEPS Pro BT, Powder BT, DSP Sport, DSP Pro, DSP Pro Ice, Micro BT Button, Micro BT Sensor and Micro BT Race avalanche transceivers and the Black Diamond branded Recon BT and Guide BT avalanche transceivers. All the transceivers are plastic with an LCD screen. They measure about 5 inches long by 3 inches wide and the colors vary by model. The transceivers have PIEPS or the Black Diamond logo printed on the front of the unit and the model name printed either on the front or rear of the unit. To verify that your unit is included in this recall, go to www.blackdiamondequipment.com/en_US/content/beacon-notification/ to verify that the switch can transition from the SEND to SEARCH mode properly.

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls 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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