Carrier Corporation

Complete recall history across all FDA and CPSC categories, 3 total recalls

Carrier Corporation 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 (3)

CPSC consumer product recalls by Carrier Corporation

Date Product Hazard
May 11, 2017 Carrier Greenspeed™ and Bryant Evolution Extreme™ Heat Pumps The capacitors in the fuse boards in the heat pumps can stop working causing the unit to overheat...
Feb 23, 2017 Packaged Terminal Air Conditioners (PTAC) and Packaged Terminal Heat Pumps (P... The power cord plug of the packaged terminal air conditioners (PTAC) and packaged terminal heat p...
Dec 22, 2015 Packaged Terminal Air Conditioners (PTAC) and Heat Pumps (PTHP) The power cord plug can overheat, posing a fire hazard to consumers.

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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