Severity
Moderate
BLU3, of Pompano Beach, Florida issued this CPSC recall on December 22, 2022. Classified as Moderate severity. Approximately About 1,300 (In addition, about 20 were sold in Canada) units are affected. The recall was issued because: The compressor head of the tankless diving system can fracture while in use resulting in restricted air flow, posing a …. 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.
This CPSC action (record #23076) was formally reported on December 22, 2022. It is classified under Moderate severity, with a current status of Active. BLU3, of Pompano Beach, Florida is listed as the recalling firm. Federal records indicate About 1,300 (In addition, about 20 were sold in Canada) units are affected, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: The compressor head of the tankless diving system can fracture while in use resulting in restricted air flow, posing a drowning hazard for divers. 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 Nomad tankless diving systems and contact BLU3 to schedule a free repair at an approved service center. BLU3 is contacting all known purchasers di… — 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, of which 6 were also issued by CPSC. 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.
Severity
Moderate
Units Affected
About 1,300 (In addition, about 20 were sold in Canada)
Related Recalls
6
6 from same agency
This recall involves BLU3's Nomad battery-powered tankless diving systems. The BLU3 logo and Nomad appear in writing on the top handle of the dive system. Consumers can identify whether their Nomad is included in the recall by contacting BLU3 and providing the serial number for their Nomad. The serial number can be found in the compartment behind the battery door. Serial numbers ending with the last four digits between 0000 to 2700 are included in the recall.
The compressor head of the tankless diving system can fracture while in use resulting in restricted air flow, posing a drowning hazard for divers.
Consumers should immediately stop using the recalled Nomad tankless diving systems and contact BLU3 to schedule a free repair at an approved service center. BLU3 is contacting all known purchasers directly. The repair cannot be performed by the consumer.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 23076 |
| Date reported | December 22, 2022 |
| Date initiated | December 22, 2022 |
| Recalling firm | BLU3, of Pompano Beach, Florida |
| Units affected | About 1,300 (In addition, about 20 were sold in Canada) |
| Distribution | Not disclosed |
Profile values are sourced directly from the official CPSC enforcement record. Source: U.S. Consumer Product Safety Commission.
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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.
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Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.
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.
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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).