PlainRecalls

AQUALUNG Recalls Buoyancy Compensator Devices Due to Injury and Drowning Hazards

Reported: October 20, 2022 Initiated: October 20, 2022 #23021 330 units

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.

Recall Insight

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.

Recall Distribution by Severity Class

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

Severity

Moderate

Units Affected

330

Related Recalls

6

0 from same agency

Recall Progress (industry avg ~60%) 60.0%

Product Description

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.

Reason for Recall

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.

Remedy

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.

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 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.

Scale of Impact

330 units affected — limited or regional distribution scale.

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

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 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.. Recalled by AQUALUNG Group, of Carlsbad, California. Units affected: 330.
Why was this product recalled?
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.
What should consumers do?
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.
Which agency issued this recall?
This recall was issued by the CPSC on October 20, 2022. Severity: Moderate. Recall number: 23021.
How do I check if my product is affected by a recall?
Check the product description and recall number (23021) 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).