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Mckesson Medical Immaging

Complete recall history across all FDA and CPSC categories — 4 total recalls

Mckesson Medical Immaging 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.

Device Recalls (4)

FDA medical device enforcement actions by Mckesson Medical Immaging

Date Product Reason Class
Feb 18, 2016 McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 1... McKesson has identified a design deficiency where under rare circumstances, i... Class II
May 29, 2014 Horizon Medical Imaging Horizon Medical Imaging is a medical image and inf... Firm received a complaint that an unreported study performed that day could n... Class II
May 5, 2014 Horizon Medical Imaging It is a medical image and information management a... The firm has identified a software issue which may cause a discrepancy betwee... Class II
Apr 17, 2014 McKesson Radiology-PACS. McKesson Radiology is a medical image and informa... High priority alert icon was not displayed in the Study List when there are n... Class II

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.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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