Medrad Inc
Complete recall history across all FDA and CPSC categories — 13 total recalls
Medrad 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.
Device Recalls (13)
FDA medical device enforcement actions by Medrad Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 15, 2013 | DC power cable (p/n 3010556) supplied with the MEDRAD(R) Veris MR Vital Signs... | The firm is recalling these power cables due to a latent design reliability i... | Class II |
| Nov 5, 2012 | MEDRAD Hand Controller Sheath, Catalog number AVA 500 HCS/3010903, for cardia... | The seal between the white polyethylene and the clear plastic may be missing ... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Secondary Set Peristaltic Pump Syst... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion Pump Peristaltic Pump System designed for ... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Primary VSA Stopcock Set Peristalti... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Standard Administration Kit Perista... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Primary Set Peristaltic Pump System... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Primary Spike Set Peristaltic Pump ... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Primary VSA Set Peristaltic Pump Sy... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Secondary VSA Set Peristaltic Pump ... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Side Step Set Peristaltic Pump Syst... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Secondary Spike Set Peristaltic Pum... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | Class II |
| Apr 18, 2012 | Medrad(R) Continuum MR Infusion System Secondary Administration Kit Perist... | Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubi... | 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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