PlainRecalls

Huish Outdoors Recalls Buoyancy Control Devices (BCDs) Due to Drowning Hazard

Reported: October 23, 2018 Initiated: October 23, 2018 #19018 About 2,600 (In addition, about 800 were sold in Canada) units

Huish Outdoors LLC, dba Zeagle, of Salt Lake City, Utah issued this CPSC recall on October 23, 2018. Classified as Moderate severity. Approximately About 2,600 (In addition, about 800 were sold in Canada) units are affected. The recall was issued because: Buttons on the Zeagle Sport BCD inflators can break or fracture leading to a rapid loss of air or auto inflation of the…. 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 #19018) was formally reported on October 23, 2018. It is classified under Moderate severity, with a current status of Active. Huish Outdoors LLC, dba Zeagle, of Salt Lake City, Utah is listed as the recalling firm. Federal records indicate About 2,600 (In addition, about 800 were sold in Canada) 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: Buttons on the Zeagle Sport BCD inflators can break or fracture leading to a rapid loss of air or auto inflation of the BCD, posing a drowning hazard to scuba 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 BCDs and call Zeagle for instructions on how to receive a free replacement. — 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 8 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 2,600 (In addition, about 800 were sold in Canada)

Related Recalls

6

0 from same agency

Product Description

This recall involves Zeagle Sport BCD inflators. BCDs are used to help a diver maintain buoyancy under water during scuba diving. Models include Sport Base, Sport Resort, Sport Base Plus, Sport Resort Plus, and Sport Focus. Serial numbers are located on the inside of BCD pocket. Affected serial numbers: 620150000 - 620150800 2015081625 - 2015080921 2016035830 - 2016034676 1030062 - 1030001 2015114475 - 2015112942 1012775 - 1012051 2015092740 - 2015091746 1011765 - 1010001

Reason for Recall

Buttons on the Zeagle Sport BCD inflators can break or fracture leading to a rapid loss of air or auto inflation of the BCD, posing a drowning hazard to scuba divers.

Remedy

Consumers should immediately stop using the recalled BCDs and call Zeagle for instructions on how to receive a free replacement.

Details

Units Affected
About 2,600 (In addition, about 800 were sold in Canada)

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 19018
Date reported October 23, 2018
Date initiated October 23, 2018
Recalling firm Huish Outdoors LLC, dba Zeagle, of Salt Lake City, Utah
Units affected About 2,600 (In addition, about 800 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.

Scale of Impact

About 2,600 (In addition, about 800 were sold in Canada) 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 Zeagle Sport BCD inflators. BCDs are used to help a diver maintain buoyancy under water during scuba diving. Models include Sport Base, Sport Resort, Sport Base Plus, Sport Resort Plus, and Sport Focus. Serial numbers are located on the inside of BCD pocket. Affected serial numbers: 620150000 - 620150800 2015081625 - 2015080921 2016035830 - 2016034676 1030062 - 1030001 2015114475 - 2015112942 1012775 - 1012051 2015092740 - 2015091746 1011765 - 1010001. Recalled by Huish Outdoors LLC, dba Zeagle, of Salt Lake City, Utah. Units affected: About 2,600 (In addition, about 800 were sold in Canada).
Why was this product recalled?
Buttons on the Zeagle Sport BCD inflators can break or fracture leading to a rapid loss of air or auto inflation of the BCD, posing a drowning hazard to scuba divers.
What should consumers do?
Consumers should immediately stop using the recalled BCDs and call Zeagle for instructions on how to receive a free replacement.
Which agency issued this recall?
This recall was issued by the CPSC on October 23, 2018. Severity: Moderate. Recall number: 19018.
How do I check if my product is affected by a recall?
Check the product description and recall number (19018) 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).