RecallHawk

Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels

Unknown Manufacturer

Summary

CPSC recalled Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels by Unknown Manufacturer. Hazard: The spring locking mechanism on the recalled avalanche shovels can fail in an emergency excavation of a person buried by an avalanche, posing a risk of injury or death for the buried person.. Remedy: Consumers should immediately stop using the recalled avalanche shovels and follow the instructions at https://mammut.prezly.com/recall-notice-for-a-call-for-inspection-shovel-locking-mechanism to inspect the connection between the shaft and the shovel head to make sure it properly locks into position. If the connection does not lock into position, consumers should contact Mammut to obtain a prepaid return shipping label to return the shovel for a free repair or a free replacement shovel..

Details

Source

cpsc

External ID

23174

Action Date

2023-04-06

Status

Ongoing

Category

product

Product Description

This recall involves Alugator Ride 3.0 Hoe and Alugator Ride SE shovels. The recalled shovels are used for digging out avalanche victims. The recalled shovels are made of aluminum, were sold in silver or black finishes and have orange handles. The recalled Alugator Ride 3.0 Hoe avalanche shovels were sold individually with production lot number 1121. The Alugator Ride SE avalanche shovels were sold as part of the Barryvox Package, and Barryvox Package Tour with production lot numbers 1221 and 0322. The product name and production lot number are printed on shovel shaft near the handle.

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.

Want to know the moment something like this happens?

Get alerts for product

Related Actions