RecallHawk

SCUBA Diving Buoyancy Compensating Devices OceanPro, Excursion, Hera

Unknown Manufacturer

Summary

CPSC recalled SCUBA Diving Buoyancy Compensating Devices OceanPro, Excursion, Hera by Unknown Manufacturer. Hazard: The handle for the weight pockets in the Scuba Diving Buoyancy Compensating Device can break during use. If this happens, the user will not be able to dump weight pockets in an emergency to rise to the surface, posing a drowning hazard.. Remedy: Consumers should immediately stop using the recalled SCUBA Diving Buoyancy Compensating Devices and contact Huish Outdoors to receive free replacement weight pockets. Pockets are detachable and easily replaceable. Consumers should dispose of the current weight pockets..

Details

Source

cpsc

External ID

23222

Action Date

2023-06-15

Status

Ongoing

Category

product

Product Description

This recall involves SCUBA Diving Buoyancy Compensating Devices (BCD). The user wears the jacket style BCD during a dive. The recalled BCDs look like a vest with an attachment point on the back for the tank, an upper airway assembly that consists of a corrugated rubber hose and an inflation mechanism that can be attached to a SCUBA regulator, and integrated weight pouches on either side that can be loaded with weights that can be dumped in an emergency. The recalled devices include the following models: Oceanic OceanPro, Oceanic Excursion, and Oceanic Hera with serial numbers: 608262 through 695909, 1170357 through 1180342, 1200001 through 1200070 and 20031001 through 22082698. Only these models in any of these serial number ranges and QLR4 Pocket Handles that DO NOT contain a date code on the underside are included in the recall. The brand name Oceanic and the model name are embroidered on the side pockets and a serial number is on the label on the inside of the jacket assembly.

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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