By HFA staff

It is important to pay attention when a product is recalled, but with all the different sources of information and the different types of recalls, it can be confusing. Recalls, designed to protect the public鈥檚 health, are used as a way to deliver information to consumers in an expeditious manner.

A recall is an action taken by a manufacturer to remove a product (food, drugs, medical devices and cosmetics) from the market, initiated either by the manufacturer or by request from the U.S. Food and Drug Administration. In either case, the manufacturer removes or corrects a product that is in the market and in violation of FDA rules and regulations. In both cases, the FDA considers the recall to be manufacturer initiated.

Alternatively, an FDA-mandated recall, also known as a mandatory recall, occurs when FDA orders a manufacturer to recall a product or mandates recall requirements. The FDA鈥檚 role is to oversee the manufacturer鈥檚 recall strategy, monitor the recall for effectiveness and classify the recall.

Recall Classification

  • Class I: Includes a health hazard situation in which there is reasonable probability that the use of the product will lead to serious, adverse health consequences or death.
  • Class II: Includes a potential health hazard situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
  • Class III: Includes a situation in which use of or exposure to the product is not likely to cause adverse health consequences.
  • Market withdrawal: When a product has a minor violation that would not be subject to FDA legal action a 鈥渕arket withdrawal鈥 occurs. The product is removed by the firm from the market or the firm corrects the violation.
  • Medical device safety alert: Released in circumstances in which a medical device may present an unreasonable risk of substantial harm. These situations also are considered recalls in certain cases.

Each FDA recall follows specific timelines and procedures depending upon the circumstances. For example, each recall is initiated with a written order that states the violation, the product, lot and serial numbers to be recalled, and the timeline for the recall. Each recall is unique and requires its own recall strategy developed by the Center Recall Unit. The CRU will consider how far the recall should extend, whether the public needs to be warned and if so, in what geographical area, and the appropriate assessment for recall effectiveness. A recall designated voluntary, requested and mandatory depends on who initiates the process. Based upon the gravity of the situation, FDA will issue a public warning.

Recall Methods

Voluntary Recall: Initiation of a Recall by a Manufacturer

Consistent with its responsibility to protect the public health from products that are defective or potentially harmful, a manufacturer may voluntarily initiate a recall. If a recall is manufacturer-initiated, FDA reviews the information provided by the manufacturer, conducts a health hazard evaluation, classifies the recall and then advises the manufacturer in writing of the assigned recall classification. FDA then places the notice of the recall in the FDA Weekly Enforcement Report. Nearly all recalls implemented in the U.S. are begun on a voluntary basis by the anything we can go to get.

If a manufacturer has voluntarily initiated a recall, it is the manufacturer鈥檚 responsibility to promptly notify each of its direct accounts. If the recall extends beyond direct accounts, then the direct accounts should be instructed by the recalling manufacturer to contact sub-accounts that may have received the product. Once all the accounts have been informed about the recall, they must promptly follow the recall strategy that was previously put in place for that account.

FDA Requested Recall

In urgent situations, FDA may request a recall. The request is directed to the manufacturer that has the primary responsibility for making or marketing the product. Class 1 category recalls are most often requested recalls. It is important to note FDA considers an FDA requested recall to be manufacturer initiated.

The associate commissioner for regulatory affairs approves all recall requests from FDA. A letter outlining the need for a recall is sent to manufacturer. After a recall has begun, the recall is entered in the Recall Enterprise System. The RES is a database used by FDA to submit, update, classify and terminate recalls.

FDA Mandated Recalls

FDA鈥檚 authority to issue a mandatory recall is very limited. Subjects of mandatory recalls can include devices, biological products, human tissue intended for transplantation, infant formula, tobacco products and food. FDA also has discretion to order a mandatory recall if it finds that a human cell, tissue or cellular or tissue-based product is a source of dangerous infection to humans or does not adequately protect against communicable disease.

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