RecallHawk

Apeks Exotec SCUBA Diving Buoyancy Compensator Devices (BCDs)

AQUALUNG Group, of Carlsbad, California

Summary

CPSC recall: Apeks Exotec SCUBA Diving Buoyancy Compensator Devices (BCDs). By AQUALUNG Group, of Carlsbad, California. Hazard: 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

Details

Source

CPSC Consumer Product Recall

External ID

9429

Action Date

2022-10-20

Status

Recalled

Category

consumer_product

Product Description

This recall involves Apeks Exotec SCUBA Diving Buoyancy Compensator Devices (BCDs). The Exotec is a back flotation-style

Context & Analysis

This is a unclassified recall.

This was one of 14 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

AQUALUNG Group, of Carlsbad, California has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (AQUALUNG Group, of Carlsbad, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does AQUALUNG Group, of Carlsbad, California have FDA actions?

AQUALUNG Group, of Carlsbad, California has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9429" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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