FDA recall

How to Stay Safe and Informed During an FDA Recall of Your Medication

Our chapter on drug recalls within Your Complete Guide to Hiring a Personal Injury Lawyer outlines just how frighteningly common FDA recall actions on pharmaceutical products are in the United States today. In that chapter, we also touched on some of the things you should do to protect yourself when your medication or other medical devices you rely on are discovered to be defective and officially recalled. 

Due to the recent—and still developing—Zantac recall, we are delving a little deeper into FDA recalls of prescription drugs and over-the-counter medicines in today’s post. 

If you’re afraid you’ve been injured or have gotten sick from taking any recalled drug, contact an experienced personal injury attorney today. In the meantime, learn more about what to do when the FDA announces a drug recall for any medication you or your loved ones currently take or have used at any time in the past. 

Get to Know the FDA’s Drug Recall Terminology 

It is important to remember that in the U.S., the federal government-based FDA (Food and Drug Administration) is typically involved in all drug recall processes. This body does not tend to act quickly. Still, it does give consumers a centralized place to find crucial public health information on drug safety issues and testing. 

If you use any medications or over-the-counter remedies, you should get to know the FDA’s drug recalls website and some specific terms and classifications they use. Taking the time to understand FDA recalls of drugs and medical devices is key to keeping yourself safe. We encourage you to review the administration’s basic FDA 101 overview information. 

Stay Safe – Stay Informed with FDA Reports on Medication Recalls 

It is essential to be aware of and remain safe regarding medication recalls. The FDA keeps track of all medication recalls, providing the public with reports as necessary. Educating yourself on accessing this information can help you stay current with any recalled drugs, supplements, or products. 

The FDA recall reports offer a comprehensive account of the recalled product, including information about the producer, distribution methods, rationale for the recall, and potential health risks. By having access to this knowledge beforehand, consumers can make an enlightened decision before ingesting a recalled medication or buying from a suspicious provider. 

Consumers can also rely on these reports to guarantee that their supplier follows safety regulations. Knowing what’s in your medications and where they come from helps protect you against the risk of consuming hazardous ingredients or becoming a victim of counterfeiting schemes. 

Thankfully, obtaining these reports is a breeze. The FDA website offers in-depth details on newly released recall notices and archives from the past few years. Furthermore, you can also find reports at local pharmacies and hospitals with ease! 

Knowing how to access FDA reports on recalls can prepare you for any unfortunate circumstances that may arise with your medications. This knowledge is power and peace of mind—something all consumers should have when purchasing medication from reliable sources! By monitoring potential issues, you can take control of your healthcare needs and rest assured, knowing that you are keeping track of possible dangers associated with medicines. 

The Different Recall Classifications 

Some recalls are indeed due to simple packaging errors, and the drugs you’ve purchased are not themselves defective or dangerous. Of course, injuries could still result from mislabeling, but the product itself is not inherently unsafe for its intended users. 

Other recalls involve (in the FDA’s words) “dangerous or defective products that predictably could cause serious health problems or death.” Note that the current Zantac/ranitidine recall, as well as the earlier Valsartan recall, both involve a chemical—NDMA—that is known to cause cancer. That fact means these particular drug recalls are some of the most critical in FDA history. 

The FDA uses a rating system to express the threat level of a given recall, with classifications between I-III (Roman numerals 1-3). We invite you to review our drug recall chapter from our previously published Complete Guide post series to get the details. A Class I recall is the most serious. In contrast, Class III recalls deal more with labeling and manufacturing law violations.  

Take Action On Voluntary Recalls For Safe Medication 

When it comes to the well-being of your household, responding swiftly and appropriately to a voluntary recall of medication is paramount. This type of precautionary measure can potentially save you from hazardous health risks that could result from consuming this drug – subsequently preventing costly medical bills and other potential adverse consequences if neglected. Protect yourself today by taking action! 

To start with, it is essential to determine if your medication has been recalled. You can check for recalls on the FDA website or through a discussion with your doctor or pharmacist. If you find that your medication has indeed been subject to recall, read all the instruction documents provided for further guidance and steps moving forward. 

Recall Strategy 

In the event of a voluntary recall, it is essential to be prepared. Start by looking into the FDA website or conversing with your pharmacist or doctor to confirm if your medication has been recalled, and read all relevant documents for further instructions on how to proceed correctly. 

Remember to take note of anything regarding alternative medications that have been recommended, and talk with your doctor about the most suitable plan. Additionally, keep any recalled medication apart from other drugs in your house. If you think it could be advantageous, consult a lawyer on any legal options available should they be necessary. 

Other Important Recalled Product Terms to Know 


This term refers to a digest-type document the FDA releases to the public each week. The document contains information on each recall according to its classification. Not all FDA recalls involve drugs or medications—the administration also recalls food and other consumable products. As the Enforcement Report‘s name suggests, it also contains information on specific actions taken by the recalling product manufacturer or the FDA itself. 


Market withdrawals occur when products violate the FDA rules in a minor way that would not be subject to FDA legal action. In these situations, the product manufacturer or other responsible party removes the product from the market or corrects the violation. Once the correction has been made, the product will typically go back on sale. 


When a medical device—something like a pacemaker or other health-related item that is not necessarily a drug—is found to present “an unreasonable risk of substantial harm,” it may gain a safety alert instead of being entirely recalled. Always be sure to look for medical device safety alerts on any devices you are currently using. 


The term “Public Notification” refers to an alert issued by the FDA that notifies the public of a voluntary drug recall. The notification will provide information regarding the recalled medication and instructions on what steps to take if you have been affected. Pay attention to any Public Notifications to protect your health and stay up-to-date on any current drug recalls that could impact your or your family’s safety. 

Check-in With Your Doctor 

When a recall occurs, your first instinct might be to immediately dispose of your medication. However, you must first speak with your doctor about your options. If you’re taking a prescription for a medical condition, it is never a good idea to stop without first consulting your doctor. As soon as you hear of a recall action regarding a medicine you take, call your doctor to discuss your options to make sure your condition is being safely managed. 

Report Any Adverse Health Reactions 

It is critical to report any adverse health reactions after taking medication to your doctor, pharmacist, or healthcare professional immediately. This will provide the medical community with valuable insight into medications’ safety and side effects. The Food and Drug Administration (FDA) also recalls any potentially harmful product for various reasons, including contamination risks, efficacy issues, inadequate instruction labels, and more. Taking steps towards understanding these risks can prevent any potential health hazard circumstances in the future. 

To ensure your safety and the safety of those around you, it is pertinent that any adverse health reaction associated with a recalled medication for a product that may be defective or potentially harmful be reported at once. By doing this before an official recall announcement, you are not only protecting yourself from future harm but also providing valuable information to medical professionals regarding medications. Taking part in this process can give peace of mind knowing that everyone’s well-being has been considered. 

Know Your Legal Rights—Call a Personal Injury Lawyer for Help 

Discovering that a medication you rely on is the subject of a significant FDA recall can be confusing and scary. And knowing whether you’re a victim of the irresponsible drug industry is not always easy. 

You may be entitled to compensation if you have suffered a severe reaction to a recalled drug or if you have health issues that may be related to a recalled drug. Contacting a compassionate, experienced personal injury lawyer for help will not cost you anything to learn more about your potential recalled and defective drugs case

Westmoreland Injury Lawyers is Western PA’s Drug Recall Resource 

Here in Greensburg, Westmoreland Injury Lawyers is the region’s best legal resource for people just like you who have been hurt by defective drugs or even medical malpractice. Our caring attorneys and staff are dedicated to friendly and personal service that alleviates confusion and fear for our valued clients. Get in touch with us today to schedule your FREE legal evaluation

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