B. Braun Medical Recalls

100 recalls found for B. Braun Medical. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical CareSite IV Sets Recalled for Backflow Risk (381,850 Units, 2025)

B. Braun Medical recalled 381,850 CareSite IV sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump after concerns about backflow and occlusion. The defect could allow medication to flow from secondary piggyback IV containers into primary IV containers and prevent priming. Hospitals and clinicians should stop using the affected devices immediately and follow recall,厂

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalled 12,225,913 CARESITE IV Sets for Backflow, Occlusion (2025)

B. Braun Medical Inc. recalled 12,225,913 CARESITE gravity IV sets and pump sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The devices may backflow medication from secondary to primary IV containers and fail to prime. Healthcare facilities and patients should stop using immediately and follow the recall instructions from the manufacturer. For refund or replacement inquiries,联系

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Anesthesia IV Set Recalled for Backflow Risk — 19,392 Units, 2025 Recall

B. Braun Medical recalled 19,392 Anesthesia IV Sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The devices present a risk of backflow of medication from secondary piggyback IV containers into the primary IV line and an inability to prime. Hospitals and providers should stop using the devices immediately and follow the manufacturer’s recall instructions.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for Backflow Risk in 65,904 Units (2025)

B. Braun Medical recalled 65,904 IV Administration Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The recall cites backflow of medication from secondary (piggyback) IV containers into primary containers and an inability to prime. Hospitals should stop using the devices immediately and follow the manufacturer's recall instructions.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall for Backflow Risk (2025)

B Braun Medical recalled 135,000 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump, sold worldwide to hospitals and other healthcare providers. The devices pose a backflow risk from secondary to primary IV containers and can fail to prime. Health care facilities should stop using the affected sets and follow the manufacturer’s recall guidance.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B BRAUN MEDICAL STREAMLINE BLOODLINE SET FOR DIALOG Recalled 1,298,454 Units (2025)

B BRAUN MEDICAL recalled 1,298,454 STREAMLINE BLOODLINE SET FOR DIALOG devices nationwide in the United States after observations of micro-air bubbles and air-in-line alarms linked to damaged arterial and venous connectors. The defect increases the risk of air entering the bloodstream during dialysis. Patients and healthcare providers should stop using this device immediately and follow the recall

B BRAUN MEDICAL
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid-Position Issue (21,270 Units)

B Braun Medical recalled 21,270 PERIFIX FX Continuous Epidural Anesthesia Tray units distributed nationwide to hospitals and surgical centers after a lid-position defect was identified in the catheter connector. The defect allows the catheter connector lid to be in the incorrect position. Healthcare facilities and clinicians should stop using the device immediately and follow the manufacturer’s or

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recall: 60-Unit Anesthesia Tray Recalled for Catheter Connector Lid Position Issue

B BRAUN MEDICAL INC recalls 60 units of SESK Combined Spinal and Epidural Tray nationwide. The recall targets products distributed to all 50 states. The defective lid on the catheter connector may be in the incorrect position, posing a high-risk device issue. Stop using immediately and follow company instructions for recall remedies.

B BRAUN MEDICAL
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical ESPOCAN Spinal/Epidural Tray Recalled Over Lid Position Risk

B Braun Medical recalled 10,130 ESPOCAN spinal/epidural trays nationwide after discovering potential for the catheter connector lid to be in an incorrect position. The recall covers multiple product codes and UDI numbers. Healthcare providers must stop using affected units and follow manufacturer instructions for remediation.

B BRAUN MEDICAL
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Tray Recalled for 0 Units in 2025

B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide. The recall centers on the lid of the catheter connector that may be in the incorrect position. Patients and healthcare providers should stop using the device immediately and follow recall instructions.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Tray Recalled for Lid Misalignment in 48,110 Units (2025)

B Braun Medical Inc. recalled 48,110 units of the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide to hospitals and surgical centers. The recall cites a potential for the lid of the catheter connector to be in the incorrect position. Hospitals and clinics should stop using the device and contact B Braun Medical for instructions.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recall Expands for Perifix FX Epidural Tray and Catheter Over Lid Position Defect (Z

B Braun Medical recalled an epidural anesthesia tray nationwide after finding a lid misalignment in the catheter connector could occur. The recall involves the PERIFIX FX Continuous Epidural Anesthesia Tray and PERIFIX FX Springwound Catheter with a 17 Ga Tuohy needle and 19 Ga closed-tip catheter. The recall date is 2025-09-18 with report of ongoing action as of 2025-10-15. Healthcare providers,,

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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical PERIFIX FX Epidural Set Recalled for Lid-Position Defect in 2025

B Braun Medical recalls the PERIFIX FX Continuous Epidural Anesthesia Set and PERIFIX Tuohy Epidural Needle nationwide after a lid-position defect is identified. The issue involves the lid of the catheter connector being in the incorrect position. Healthcare providers are advised to stop using the device and follow the manufacturer’s recall instructions.

B Braun Medical
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Health & Personal Care
HIGH
FDA DRUG

B. Braun Lactated Ringers Injection 46,032 Containers Recalled Over Particulate Matter

B. Braun Medical recalled 46,032 containers of Lactated Ringers Injection USP sold nationwide in the United States. The recall cites the presence of particulate matter in the 1000 mL IV solution. Consumers should stop using the product immediately and contact their healthcare provider or B. Braun for guidance.

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Brand Statistics

Total Recalls
100
Pages
5

Related Brands

B Braun MedicalB BRAUN MEDICALLactated Ringers