Specialized Bicycle Components Inc.

Complete recall history across all FDA and CPSC categories, 5 total recalls

Specialized Bicycle Components Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Product Recalls (5)

CPSC consumer product recalls by Specialized Bicycle Components Inc.

Date Product Hazard
Jul 15, 2015 Pedal Axle Extenders The Pedal Axle Extenders can break, and the rider can lose control, posing a fall hazard.
Jun 21, 2006 Bicycles with SW Carbon Stem with Magnesium Faceplate The bicycle's stem has a magnesium faceplate that holds the handlebar in place. The faceplates on...
Sep 28, 2004 Allez Sport, Allez Elite, Roubaix, and Sequoia Bicycles The handlebar may loosen and turn unexpectedly, which can cause the rider to lose control and fall.
Dec 9, 2003 Specialized mountain bikes During heavy braking, the brake tabs on the front forks could break off, possibly causing a loss ...
Jun 8, 1998 Chains on Specialized bicycles The chains on these bicycles were produced with a malfunctioning chain assembly tool. These chain...

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious, there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious, the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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