PlainRecalls

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 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) units

CPSC recall on July 28, 2022. Classified as Moderate severity. Approximately 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) units are affected. The recall was issued because: The recalled transceivers may not switch from SEND mode into SEARCH mode. If this were to occur, the device would not b…. This recall notice is sourced from official CPSC enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This CPSC action (record #22194) was formally reported on July 28, 2022. It is classified under Moderate severity, with a current status of Active. The recalling firm is not specified in the federal record. Federal records indicate 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) units are affected, placing this recall in the million-unit bracket that typically triggers nationwide consumer alerts and retailer sweeps.

The documented reason for this recall is: 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 s… Distribution information was not included in the agency filing, so consumers should assume broad potential exposure until the firm publishes point-of-sale details. The remedy documented by the agency is: 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 devi… — consumers holding this product should act on that instruction rather than relying on general guidance.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 4 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Moderate

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)

Related Recalls

6

0 from same agency

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)

Recall Profile

Structured summary of the CPSC recall record
Attribute Value
Agency U.S. Consumer Product Safety Commission
Severity class Moderate
Status Active
Recall number 22194
Date reported July 28, 2022
Date initiated July 28, 2022
Recalling firm Not disclosed
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)
Distribution Not disclosed

Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.

Scale of Impact

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) units affected — million-unit bracket.

Regional (<10K units)
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units) ✓ This recall

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Consumer Product Safety Commission filings.

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.
How do I check if my product is affected by a recall?
Check the product description and recall number (22194) against your product. Visit the official CPSC website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
How do I report an injury from a recalled product?
Report injuries to the issuing agency: CPSC at SaferProducts.gov, NHTSA at nhtsa.gov/report-a-safety-problem, or FDA via MedWatch. Document the product (photos, model/serial numbers, purchase receipts) and seek medical attention. Injury reports help agencies track hazard patterns and may strengthen enforcement actions.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as moderate severity, indicating the product may cause temporary or medically reversible health consequences. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with Endo-Model Replacement Plateau; Item Number: 15-0027/11; →

Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).