425 recalls tagged with “burn risk”.
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 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 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 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 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 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 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 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 10,896 IV administration sets on October 29, 2025. The recall addresses a risk of medication backflow from secondary IV containers. This issue could lead to serious health risks for patients.
B Braun Medical recalled 31,392 IV administration sets on October 29, 2025, due to a high risk of medication backflow. The affected models include catalog number 490301. This recall affects devices distributed worldwide, including the US and Canada.
B Braun Medical recalled 9,500 IV administration sets on October 29, 2025, due to a risk of medication backflow. The recall affects models used in conjunction with the Infusomat Space, Outlook, and Vista Basic pumps. Healthcare providers and patients must stop using these devices immediately to avoid serious health risks.
B Braun Medical recalled 126,050 IV administration sets on October 29, 2025. The recall affects devices used with the Infusomat Space, Outlook, and Vista pumps. Users face a high risk of medication backflow and occlusions.
B Braun Medical recalled 135,000 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers. Healthcare providers must stop using the device immediately.
B Braun Medical recalled 129,480 IV administration sets on October 29, 2025. The recall follows reports of potential backflow of medication from secondary IV containers into primary containers. Patients and healthcare providers must stop using the devices immediately.
B Braun Medical recalled 32,436 Anesthesia IV Sets on October 29, 2025. The recall affects specific catalog numbers due to a risk of medication backflow. Healthcare providers must stop using these devices immediately and follow the provided recall instructions.
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 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 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.
Medline Industries recalled 182,526 units of CURAD Germ-Shield Touch-Free Fabric Bandages due to compromised sterility. The recall affects all lots manufactured and distributed in the US, Guam, Canada, and the UAE. Consumers must stop using these bandages immediately.
Medline Industries recalled 11,291,800 units of Quick Strip Fabric Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals that compromise sterility. Consumers should stop using these bandages immediately.