- Find Regulatory Requirements for your country
- GHTF
- Validation Requirements
- Medical Device Software
- Sterilization
|
SUBSCRIBE (always Free) |
|
What is a “recall” as defined by the FDA?
Removal or correction of products that are in violation of laws administered by the Food and Drug Administration
Action taken by manufacturers and distributors to "protect the public health and well-being from products that present a risk of injury or gross deception or are otherwise defective."