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News & Knowledge

Georgia Handbook: Medical Product Recalls

HOW WILL WE KNOW IF A DRUG OR A PRODUCT WE USE IS RECALLED?

Occasionally, drugs and medical products are recalled or become the subject of “safety alerts” issued by the U.S. Food and Drug Administration (FDA). Medical practices often receive calls from patients who hear about such events on the news or read about them on the web. If you are enrolled in the PDR Network, you will receive notice of the recall or safety alert. To learn more about the PDR Network, visit www.pdr.net or call the Risk Management Department at Curi.
If you have not heard about the recall and a patient brings the issue to your attention, you first must determine whether the product really has been recalled or is simply being studied due to reports of adverse…

Curi’s risk mitigation resources and guidance are offered for educational and informational purposes only. This information is not medical or legal advice, does not replace independent professional judgment, does not constitute an endorsement of any kind, should not be deemed authoritative, and does not establish a standard of care in clinical settings or in courts of law. If you need legal advice, you should consult your independent/corporate counsel. We have found that using risk mitigation efforts can reduce malpractice risk; however, we do not make any guarantees that following these risk recommendations will prevent a complaint, claim, or suit from occurring, or mitigate the outcome(s) associated with any of them.

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