Mckesson Information Solutions LLC

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

Mckesson Information Solutions LLC 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 (5)

FDA medical device enforcement actions by Mckesson Information Solutions LLC

Date Product Reason Class
Aug 27, 2014 McKesson Cardiology" Hemo intended for complete physiological/hemodynamic mon... Software Error: The McKesson Cardiology Hemo calculation section incorrectly ... Class II
Jun 25, 2014 McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for comple... McKesson Cardiology Hemo front-end parameter boxes must undergo annual maint... Class II
Dec 23, 2013 Horizon Medical Imaging, Picture Archive Communication System (PACS). Images may be archived to an incorrect or invalid archive location resulting ... Class II
Oct 15, 2013 McKesson Radiology 12.0, Picture Archiving Communication System (PACSA). When merging two patient records into one patient record using McKesson Radio... Class II
Sep 4, 2013 McKesson Horizon Medical Imaging (HMI) Radiological Image Processing System, ... Software malfunction may occur resulting in a certain combination of server c... 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.

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