RecallHawk

Shell Diving Inflation Valves with Int'l Nipples for diving dry suits

SI Tech, of Sweden

Summary

CPSC recalled Shell Diving Inflation Valves with Int'l Nipples for diving dry suits by SI Tech, of Sweden. Hazard: The internal part in the valve can malfunction while in use, causing loss of inflation and thermal protection, posing a risk of hypothermia to the consumer.. Remedy: Consumers should immediately stop using the dry suits with the recalled inflation valve and contact Ocean Equipment to receive a notification form and shipping information to return the recalled valve free of charge. The valve part will be replaced by trained technicians who are exclusively authorized to update the valve with a free replacement valve part..

Details

Source

cpsc

External ID

22115

Action Date

2022-04-14

Status

Ongoing

Category

product

Product Description

This recall involves the Shell Inflation Valves with Int'l Nipples that come with diving dry suits and are also sold separately. The Shell Inflation Valve is used in recreational and technical diving. The recalled valve inflates the diving dry suit to allow the diver to equalize air pressure while descending in the water by pressing on the valve and it provides thermal protection to the diver. The model number and batch code are stamped on the inside of the recalled valve. Instructions on how to find and identify the batch code can be found at www.sitech.se. Model Number 25210 JD1, JE2, JE5, JE6, JF6, JG2, JK6, JK9, JKA, JL1, JL3, KA7, KB8, KG2, KH3, KH4, KK7, KL3, LC1, LC2, LC4, LC7, LC9, LD2, LD6, LD7, LD8 25215 JG1, KA9, LC5

Context & Analysis

SI Tech, of Sweden has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

How often does SI Tech, of Sweden have FDA actions?

SI Tech, of Sweden 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. 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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