101 recalls found for B. Braun Medical. Check if any of your products are affected.
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.
B Braun Medical recalled 46,250 IV administration sets on October 29, 2025. The recall follows concerns about potential backflow of medication into primary IV containers. The affected products were sold worldwide, including the US and Canada.
B Braun Medical recalled 11,832 IV administration sets on October 29, 2025. The recall affects models catalog numbers 490315, 490331, and 490376. The device poses a risk of medication backflow and occlusion during use.
B Braun Medical recalled 187,464 IV administration sets on October 29, 2025. The recall stems from the potential for medication backflow and occlusion. The affected products were distributed worldwide, including the U.S. and Canada.
B Braun Medical recalled 150,664 IV administration sets on October 29, 2025. The recall affects products identified by catalog number 375258. These devices pose a high risk of medication backflow from secondary IV containers.
B Braun Medical recalled 18,072 IV administration sets on October 29, 2025. The recall affects the Outlook set utilized with Infusomat Space and Outlook Pumps. The sets pose a high risk of medication backflow and priming issues.
B BRAUN MEDICAL recalled 1,298,454 hemodialysis bloodlines on September 30, 2025. The recall results from the risk of micro-air bubbles due to damaged connectors. Patients should stop using the product immediately and follow the manufacturer’s instructions.
B BRAUN MEDICAL recalled 21,270 epidural anesthesia trays on September 18, 2025. The recall follows concerns about a potential misalignment of the catheter connector lid. Patients and healthcare providers must stop using the device immediately.
B Braun Medical recalled 48,110 epidural anesthesia trays on September 18, 2025. The recall stems from a potential issue with the catheter connector lid. Healthcare providers and patients must stop using the device immediately.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects a potential defect in the catheter connector lid. Patients and healthcare providers must stop using the device immediately.
B Braun Medical recalled 5,770 PERIFIX FX Epidural Anesthesia Trays on September 18, 2025. The recall stems from a potential issue with the lid of the catheter connector. This defect may cause improper operation during procedures, posing serious health risks.
B Braun Medical recalled 2,450 pain management trays on September 18, 2025. The recall stems from a potential issue with the catheter connector lid positioning. This defect poses a high risk to patient safety.
B BRAUN MEDICAL recalled its PERIFIX FX Continuous Epidural Anesthesia Set on September 18, 2025. The recall affects a potential defect in the catheter connector lid position. This high-risk issue could impact patient safety in healthcare settings across the country.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The manufacturer identified a potential issue with the catheter connector lid position. No injuries have been reported, but users should stop using the product immediately.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects an unspecified number of units due to a potential connector misalignment. This issue poses a high risk to patient safety and requires immediate action from healthcare providers.
B Braun Medical recalled 2,760 units of its PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall stems from a potential misalignment of the catheter connector lid, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately and follow the manufacturer’s instructions.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray on September 18, 2025. The recall affects a potential safety issue with the catheter connector. No injuries have been reported but the hazard level is classified as high.
B Braun Medical recalled 2,840 anesthesia trays on September 18, 2025. The recall stems from a potential defect in the catheter connector lid position. The product poses a high hazard risk to patients and healthcare providers.
B Braun Medical recalled 60 units of its Combined Spinal and Epidural Anesthesia Tray on September 18, 2025. The recall stems from the potential for the lid of the catheter connector to be incorrectly positioned. Healthcare providers must stop using the device immediately and follow manufacturer instructions.
B Braun Medical recalled 10,130 units of its Combined Spinal and Epidural Anesthesia Tray on September 18, 2025. The recall affects devices due to a potential misalignment with the catheter connector lid. Healthcare providers and patients must stop using the product immediately.