What are FDA adverse event reports for Lectins And Protectins?

The FDA's MAUDE (Manufacturer and User Facility Device Experience) database collects reports of adverse events involving medical devices. For Lectins And Protectins, there are 701 total reports including 0 death reports and 0 injury reports. These reports are submitted by manufacturers, healthcare facilities, and patients. A high number of reports does not necessarily mean a device is unsafe, widely used devices naturally generate more reports.

How should I interpret MAUDE data for Lectins And Protectins?

MAUDE reports are raw adverse event submissions, not confirmed safety findings. A report that a device was involved in a death does not mean the device caused the death. Reports vary in quality and completeness. The FDA uses MAUDE data as one input among many in its safety surveillance, it does not draw conclusions from individual reports. Always consult your healthcare provider about device safety questions.

2025 data Public-data reference. official source

Lectins And Protectins

Name: Lectins And Protectins - FDA MAUDE Adverse Event Reports
Creator: PlainHospital
License: https://creativecommons.org/publicdomain/zero/1.0/

Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.

Compiled byPlainHospital Editorial, Hospital Quality Editorial Team · May 15, 2026

Open-data reference.

PlainHospital home → About this data

FDA MAUDE adverse event data · 2016–2025

What the Data Shows About Lectins And Protectins

The FDA MAUDE database aggregates 701 adverse-event reports for Lectins And Protectins spanning the period from 2016 through 2025. Of these, 0 are classified as death reports, 0 as injury reports, and 701 as malfunction reports under FDA adverse-event categorization rules. Report counts do not by themselves indicate a device is unsafe, widely used devices and longer market histories naturally generate larger raw counts, so proportional and comparative reads are more informative than totals alone.

The adverse-event profile breaks down across 1 distinct event type and 1 reported patient-outcome category, giving a multi-dimensional view that goes beyond a single headline number. A total of 2 distinct product-problem codes appear in the reports, with Incorrect, Inadequate or Imprecise Result or Readings topping the list at 700 reports. Reports are associated with 2 different manufacturers in the MAUDE record, reflecting both OEMs and repackagers of this device category.

Annual reporting volume is tracked across 2 years of MAUDE data, with the peak single-year volume reaching 700 reports - trend shape often reflects changes in device adoption, reporting rules, or FDA enforcement focus rather than underlying device behavior alone. Events are documented across 2 reported care-setting categories (hospital, home, ambulatory surgery center, etc.). All figures reflect the openFDA MAUDE snapshot last refreshed on 2026-05-15. This page is informational and is not medical advice, discuss device-safety questions with your healthcare provider.

701

Total Reports

Death Reports

Injury Reports

701

Malfunctions

Event Types

Malfunction 701 (100.0%)

Patient Outcomes

701 (100.0%)

Yearly Trend

2016: 1

2025: 700

Top Manufacturers

BECTON DICKINSON GMBH 700

IMMUCOR, INC. 1

Event Locations

700 (99.9%)

I 1 (0.1%)

Compare BECTON DICKINSON GMBH vs IMMUCOR, INC. →

Data Source

FDA Manufacturer and User Facility Device Experience (MAUDE) database via the openFDA API. Reports are submitted by manufacturers, healthcare facilities, and patients. Report counts do not indicate a device is unsafe, higher-use devices naturally generate more reports.

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Disclaimer: This information is provided for informational purposes only and does not constitute professional advice. Data is sourced from the FDA MAUDE database. Consult a qualified professional before making decisions based on this data.

Read our methodology - how this data is sourced, computed, and verified.

Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. This page draws directly on federal source data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.