Which of the following is NOT a standard requirement during a Class I medical device or pharmaceutical recall in the United States?

In the medical and pharmaceutical industry, product recalls can be critical to patient safety. The FDA classifies recalls into different categories based on risk levels, and pharmaceutical companies must follow strict protocols to ensure patient well-being. How well do you understand the standards and procedures surrounding medical product recalls? Test your knowledge with this trivia question about recall management in medicine.

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Notifying all healthcare facilities that received the product within 24 hours
Publishing recall notices in at least three national medical journals
Submitting a recall strategy to the FDA for review and approval
Establishing a system to verify that all recipients received the recall notification