PlainRecalls
CPSC Moderate Active

Black Diamond Equipment Recalls PIEPS and Black Diamond Avalanche Transceivers Due to Risk of Loss of Emergency Communications

Reported: July 28, 2022 Initiated: July 28, 2022 #22194

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.

Reason for Recall

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

Units Affected
About 76,300 (In addition, about 21,300 were sold in Canada) (Pieps DSP Sport, DSP Pro, and DSP Pro Ice avalanche transceivers were previously recalled on April 12, 2021)
Official Source
https://www.cpsc.gov/Recalls/2022/Black-Diamond-Equipment-Recalls-PIEPS-and-Black-Diamond-Avalanche-Transceivers-Due-to-Risk-of-Loss-of-Emergency-Communications

Frequently Asked Questions

What product was recalled? ▼
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.. Units affected: About 76,300 (In addition, about 21,300 were sold in Canada) (Pieps DSP Sport, DSP Pro, and DSP Pro Ice avalanche transceivers were previously recalled on April 12, 2021).
Why was this product recalled? ▼
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.
What should consumers do? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the CPSC on July 28, 2022. Severity: Moderate. Recall number: 22194.

Related Recalls

FDA Devices Moderate

Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…

Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate

COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…

Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate

Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…

Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate

Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…

Fujirebio Diagnostics, Inc. · 2026-02-11

Explore Related Data

Vehicle Safety → Drug Information →