1,425 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
B Braun Medical recalled 1,861,111 IV administration sets on October 29, 2025. The recall addresses a significant risk of medication backflow from secondary IV containers into primary containers. Healthcare providers and patients must stop using the devices immediately.
B Braun Medical recalled 1,080 IV administration sets on October 29, 2025. The recall affects sets used with the Infusomat Space, Outlook, and Vista Basic Pumps. The company identified a risk of backflow of medication from secondary IV containers into primary containers.
B Braun Medical recalled 29,900 IV Administration Sets on October 29, 2025. The recall follows reports of potential medication backflow and inability to prime. Healthcare providers and patients must stop using the device immediately.
B Braun Medical recalled 19,104 IV administration sets on October 29, 2025. The recall stems from a potential for medication backflow and inability to prime. The affected sets were distributed worldwide, including the US and Canada.
B Braun Medical recalled 27,480 IV extension sets on October 29, 2025. The recall affects devices tied to the Infusomat Space, Outlook, and Vista pumps. The company warns of potential medication backflow and occlusion issues that could endanger patients.
B Braun Medical recalled 300 IV administration sets on October 29, 2025, due to a risk of medication backflow. The defect affects the ability to prime IV containers. Healthcare providers should stop using these devices immediately.
B Braun Medical recalled 15,250 IV Administration Sets on October 29, 2025. The recall stems from a potential for medication backflow from secondary IV containers into primary IV containers. Healthcare providers and patients should stop using these devices immediately.
B Braun Medical recalled 4,488 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers. This issue may affect patient safety and requires immediate action from healthcare providers and patients.
B Braun Medical recalled 65,232 IV administration sets on October 29, 2025. The recall addresses a potential backflow risk of medication from secondary IV containers. Healthcare providers must stop using the devices immediately and follow manufacturer instructions.
B Braun Medical recalled 960 IV administration sets on October 29, 2025. The recall affects sets used with Infusomat Space, Outlook, and Vista pumps. Users face a high risk of medication backflow and occlusion.
B Braun Medical recalled 1,200 IV extension sets on October 29, 2025. The recall stems from a risk of medication backflow from secondary IV containers into primary containers. The affected model is catalog number 490358.
B Braun Medical recalled 61,423 IV administration sets on October 29, 2025, due to a high risk of medication backflow. The recall affects models with catalog numbers 456521 and 456522, distributed worldwide. Patients and healthcare providers must stop using these devices immediately.
B Braun Medical recalled 5,900 IV Administration Sets on October 29, 2025. The sets pose a risk of medication backflow and occlusion. Healthcare providers must stop using the devices immediately and follow recall instructions.
B Braun Medical recalled 162,648 IV administration sets on October 29, 2025. The products pose a high risk of backflow from secondary IV containers into primary containers. Affected sets include catalog number 354212, distributed worldwide.
B Braun Medical recalled 111,312 IV administration sets due to a risk of backflow of medication. The sets are used with Infusomat Space, Outlook, and Vista Basic Pump models. The recall was announced on October 29, 2025, following potential safety issues.
B Braun Medical recalled 286,400 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary IV containers. Users must stop using the devices immediately and follow the manufacturer's instructions.
B Braun Medical recalled 6,768 IV administration sets on October 29, 2025. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. The recall addresses a potential backflow issue that could compromise patient safety.
B Braun Medical recalled 74,652 IV administration sets on October 29, 2025. The recall impacts users of the Infusomat Space, Outlook, and Vista Basic Pumps due to backflow risks. The affected catalog number is US9923F, with worldwide distribution including the US and Canada.
B Braun Medical recalled over 20 million IV administration sets on October 29, 2025. The recall stems from a potential backflow of medication that could put patients at risk. Healthcare providers and patients must stop using the devices immediately.
B Braun Medical recalled 40,992 IV administration sets on October 29, 2025. The recall addresses a potential for backflow of medication from secondary IV containers into primary containers. This issue may lead to serious health risks for patients.
B Braun Medical recalled 13,600 IV administration sets on October 29, 2025. The recall affects models catalog number 490202 due to a potential backflow hazard. Healthcare providers and patients should stop using the devices immediately.
B Braun Medical recalled 41,016 IV administration sets on October 29, 2025. The recall addresses the risk of medication backflow into primary IV containers. This issue could lead to significant health risks for patients receiving intravenous therapy.
B Braun Medical recalled IV Administration Sets on October 29, 2025, due to a backflow risk. The recall affects devices used with Infusomat Space, Outlook, and Vista Basic Pumps. Healthcare providers should stop using the product immediately.
B Braun Medical recalled 12,320 burette sets on October 29, 2025, due to a risk of medication backflow. This defect can lead to serious health risks for patients. The recall affects devices distributed worldwide, including the U.S., Canada, Germany, Guatemala, and Singapore.
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