Boston Scientific Corp
Complete recall history across all FDA and CPSC categories — 7 total recalls
Boston Scientific Corp 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 (7)
FDA medical device enforcement actions by Boston Scientific Corp
| Date | Product | Reason | Class |
|---|---|---|---|
| Nov 20, 2015 | IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 OUS; Material Numbe... | During routine monitoring of complaints, BSC noted that the IntellaTip MiFi X... | Class II |
| Nov 20, 2015 | IntellaTip MiFi XP Asymmetric (N4) Curve, 7/110/2.5/8-8 OUS; Material Numbe... | During routine monitoring of complaints, BSC noted that the IntellaTip MiFi X... | Class II |
| Nov 20, 2015 | IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-10 ; Material Number: ... | During routine monitoring of complaints, BSC noted that the IntellaTip MiFi X... | Class II |
| Nov 20, 2015 | IntellaTip MiFi XP Asymmetric (N4) Curve 7/110/2.5/8-8 Material Number: M00... | During routine monitoring of complaints, BSC noted that the IntellaTip MiFi X... | Class II |
| Sep 11, 2015 | One Step Button, Low Profile Initial Placement PEG Kit, gastro-enterostomy tube. | Boston Scientific Corp. initiated a voluntary recall of specific lots of the ... | Class II |
| Feb 3, 2015 | IntellaTip MiFi Open-Irrigated radiofrequency Ablation Catheters: Material n... | Reports of formation of char adherent to the proximal part of the distal tip ... | Class I |
| Nov 20, 2014 | IntellaMap Orion High Resolution Mapping Catheter; Material number: M004RC64... | Some IntellaMap Orion High Resolution Mapping Catheters are exhibiting a fail... | 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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