RecallHawk

Shimano PRO Vibe Alloy stems for road bicycles

Shimano Europe B.V., of the Netherlands

Summary

CPSC recall: Shimano PRO Vibe Alloy stems for road bicycles. By Shimano Europe B.V., of the Netherlands. Hazard: The recalled bicycle stems can crack and break while in use and cause the rider to lose control, posing a risk of injury to the user in a crash.. Remedy: Consumers should immediately stop using bicycles with PRO Vibe alloy handlebar stems and take them to the place where purchased or a Shimano authorized retailer to determine if the stem on their bike is included in the recall and for

Details

Source

CPSC Consumer Product Recall

External ID

9629

Action Date

2023-05-18

Status

Recalled

Category

consumer_product

Product Description

This recall involves PRO Vibe Stem (Alloy) model black bicycle stems for road bicycles. The PRO Vibe stems were sold sep

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.

Shimano Europe B.V., of the Netherlands 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 (Shimano Europe B.V., of the Netherlands) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Shimano Europe B.V., of the Netherlands have FDA actions?

Shimano Europe B.V., of the Netherlands 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 "9629" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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