RecallHawk

YETI soft coolers and gear cases

Unknown Manufacturer

Summary

CPSC recalled YETI soft coolers and gear cases by Unknown Manufacturer. Hazard: The magnet-lined closures can fail and result in detached magnets, posing a risk of serious injury or death if ingested. When two or more high-powered magnets are swallowed, the ingested magnets can attract to each other, or to another metal object, and become lodged in the digestive system. This can result in perforations, twisting and/or blockage of the intestines, infection, blood poisoning and death.. Remedy: Consumers should immediately stop using the recalled products and contact YETI to receive a full refund or replacement product. Visit www.yeti.com for instructions on returning the product free of charge for the choice of a suggested replacement product of equal or greater value or full refund in the form of a YETI gift card with an additional $25 value..

Details

Source

cpsc

External ID

23145

Action Date

2023-03-09

Status

Ongoing

Category

product

Product Description

This recall involves the YETI Hopper M30 Soft Cooler 1.0 and 2.0, Hopper M20 Soft Backpack Cooler and SideKick Dry Gear Case. The products have a main-pocket closure lined with high-powered magnets, which are enclosed in a heat-sealed plastic strip. The M20 Soft Backpack Cooler measures about 18 inches wide and 18 inches high; the M30 Soft Cooler 1.0 and 2.0 is about 25 inches wide and 17 inches high; and the SideKick Dry Gear Case is about 11 inches wide and 7 inches high. The recalled coolers and gear cases were sold in a variety of colors and with the brand name YETI displayed on the front. A hang tag with the product name is attached to the coolers and gear cases.

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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