Yeti Link Expansion Modules and EC8 Cables
Summary
CPSC recalled Yeti Link Expansion Modules and EC8 Cables by Unknown Manufacturer. Hazard: The connection between the Yeti Link Expansion modules and the cables can overheat and melt, posing fire and burn hazards.. Remedy: Consumers should immediately stop using the recalled Yeti Link modules and cables, and contact Goal Zero to receive a free replacement kit. The kit includes a new Yeti Link module and all the necessary cables with a new connector and instructions. Goal Zero will mail a box and prepaid postage to each consumer who registers at www.goalzero.com/pages/notices-recalls. All replacement kits will be mailed to consumers after they have returned the recalled module. All cables can be discarded in the household trash. Goal Zero is contacting all known purchasers..
Details
Source
cpsc
External ID
24270
Action Date
2024-06-20
Status
Ongoing
Category
product
Product Description
This recall involves Yeti Link Expansion Modules along with EC8 power cables. They were sold as kits and also sold separately. The modules and cables were used in homes and installed in vehicles. For vehicles, the module allows consumers to wire the modules to the vehicle alternator to enable the battery to charge while the vehicle is running. In homes, the modules and cables allow consumers to connect additional batteries to the Yeti Power Station/Generator. Yeti Link Modules with model number 98200 or 98210 and Goal Zero are printed on the module. Recalled Product Name Model Number Yeti Link Expansion Module 98200 and 98210 Male EC8 to Ring Cable 98203 and 98204 Female EC8 to Ring Cable 98202 and 98205 MPPTx to Tank Cable with EC8 connector 98410 12' EC8 Extension Cable 98201 and 98206
Company
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.
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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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