RecallHawk

Vitamix Ascent® Series and Venturist® Series 8-ounce and 20-ounce Blending Containers and Blade Bases

Vita-Mix Corporation, of Cleveland, Ohio

Summary

CPSC recall: Vitamix Ascent® Series and Venturist® Series 8-ounce and 20-ounce Blending Containers and Blade Bases. By Vita-Mix Corporation, of Cleveland, Ohio. Hazard: The containers can separate from the blade base, exposing the blades, posing a laceration hazard to consumers.. Remedy: All consumers, including consumers who participated in the 2018 recall, should immediately stop using the recalled 8-ounce and 20-ounce blending containers and blade bases, and contact Vitamix for a repair kit c

Details

Source

CPSC Consumer Product Recall

External ID

9982

Action Date

2024-06-20

Status

Recalled

Category

consumer_product

Product Description

This recall involves all Ascent and Venturist Series 8-ounce blending containers, 20-ounce blending containers, and blad

Context & Analysis

This is a unclassified recall.

This was one of 18 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Vita-Mix Corporation, of Cleveland, Ohio has 2 FDA actions in our database, including 1 recall.

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 (Vita-Mix Corporation, of Cleveland, Ohio) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vita-Mix Corporation, of Cleveland, Ohio have FDA actions?

Vita-Mix Corporation, of Cleveland, Ohio 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. Search for "9982" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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