Underwater Communication Devices
Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California
Summary
CPSC recall: Underwater Communication Devices. By Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California. Hazard: Water can leak into the recalled underwater communication device during a dive and penetrate into the battery pack, causing the battery circuit board to short and ignite after the dive, posing a fire hazard.. Remedy: Consumers should immediately stop using the recalled Powercom, MilCom and RBLi-4 communication devices, remove the battery and conta
Details
Source
CPSC Consumer Product Recall
External ID
9360
Action Date
2022-07-28
Status
Recalled
Category
consumer_product
Product Description
This recall involves the PowerCom 3000D, 5000D and MilCom 6000D underwater communication devices sold with the RBLi-4 Li
Context & Analysis
This is a unclassified recall.
This was one of 15 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
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 (Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California have FDA actions?
This is the only FDA action we have on record for Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "9360" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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