Severity
Moderate
AQUALUNG Group, of Carlsbad, California issued this CPSC recall on October 20, 2022. Classified as Moderate severity. Approximately 330 units are affected. The recall was issued because: The dump valve knob can get stuck when the recalled BCD is inflated, opening the dump valve which stops the BCD from fu…. 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 #23021) was formally reported on October 20, 2022. It is classified under Moderate severity, with a current status of Active. AQUALUNG Group, of Carlsbad, California is listed as the recalling firm. Federal records indicate 330 units are affected.
The documented reason for this recall is: The dump valve knob can get stuck when the recalled BCD is inflated, opening the dump valve which stops the BCD from fully inflating. This can result in a loss of buoyancy control and poses injury (decompression sicknes… 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 buoyancy compensator devices and take them back to the place where purchased for a free repair. If a consumer is unable to return the product to a… — 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.
Severity
Moderate
Units Affected
330
Related Recalls
6
0 from same agency
This recall involves Apeks Exotec SCUBA Diving Buoyancy Compensator Devices (BCDs). The Exotec is a back flotation-style BCD used to control a SCUBA diver's buoyancy underwater. The Apeks brand and Exotec model name are embroidered on the back panel and side pockets of the BCD and the metal components are gray or orange. Only model numbers BT1380108ML, BT1380108XLXXL, BT1380110ML and BT1380110XLXXL are included in the recall. The model number is printed on the label tucked behind the bladder between the tank attachment belt and the lower dump valve.
The dump valve knob can get stuck when the recalled BCD is inflated, opening the dump valve which stops the BCD from fully inflating. This can result in a loss of buoyancy control and poses injury (decompression sickness) and drowning hazards.
Consumers should immediately stop using the recalled buoyancy compensator devices and take them back to the place where purchased for a free repair. If a consumer is unable to return the product to a dealer where purchased, they should reach out to AQUALUNG directly for instructions to receive a free repair.
| Attribute | Value |
|---|---|
| Agency | U.S. Consumer Product Safety Commission |
| Severity class | Moderate |
| Status | Active |
| Recall number | 23021 |
| Date reported | October 20, 2022 |
| Date initiated | October 20, 2022 |
| Recalling firm | AQUALUNG Group, of Carlsbad, California |
| Units affected | 330 |
| 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).