← 483 OBSERVATION EXPLORER

FDA 483 OBSERVATION · #401 OF 1,000 MOST-CITED

Report of risk to health

FDA cited this observation 49 times across 48 firms in recent inspections. Below: how it breaks down by program area and fiscal year, and real examples of how FDA worded it on Form FDA 483.

BY PROGRAM AREA
Devices49
BY FISCAL YEAR
FY20262
FY20259
FY20244
FY20239
FY20226
FY20213
FY20202
FY20192
FY20188
FY20174

How FDA worded it — real examples

A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA.

Gentuity, LLC · Sudbury, Massachusetts · Devices · 2026-03-05

A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA.

Intuitive Surgical, Inc. · Sunnyvale, California · Devices · 2025-11-05

A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA.

Abiomed, Inc. · Danvers, Massachusetts · Devices · 2025-08-05

A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA.

ASP Global, LLC. · Austell, Georgia · Devices · 2025-08-01

A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA.

Omnia Medical · Morgantown, West Virginia · Devices · 2025-07-28

A correction or removal, conducted to reduce a risk to health posed by a device, was not reported in writing to FDA.

Chamberlain Technologies LLC · Deer Park, Illinois · Devices · 2025-05-09

Related SPEQ references

Where to read the requirements behind this observation area on SPEQ. These are SPEQ's topic and audience pages — not an FDA classification of the citation.

Quality risk managementMedical devices

Examples are a representative sample of FDA's published inspection observations. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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