B. Braun Medical Recalls

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

Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall 2025 Affects 259,392 Units

B. Braun Medical recalled 259,392 IV administration sets worldwide on Oct. 29, 2025. The devices could allow backflow of medication from secondary (piggyback) IV containers into primary IV containers and may not prime due to occlusion. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions in the notice.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall for 5,952 Units Over Backflow Risk (2025)

B. Braun Medical Inc. recalled 5,952 IV Administration Sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore, for use with Infusomat Space, Outlook, and Vista Basic Pumps. The units carry Catalog Number 490612. The recall cites potential backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare teams

B. Braun Medical
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Health & Personal Care
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FDA DEVICE

B Braun Medical Recalls 98,568 IV Administration Sets for Backflow and Occlusion Risk (2025)

B Braun Medical recalled 98,568 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall covers catalog number 490274 and UDI-DI codes. The device presents a backflow risk and inability to prime. Hospitals and patients should stop using the device immediately and follow the manufacturer’s recall instructions.

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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall for 45,288 Units Over Backflow Risk (2025)

B. Braun Medical has issued an active recall for 45,288 IV administration sets catalog 490412. The devices support gravity and pump-based IV administration with Infusomat Space, Outlook, and Vista Basic Pumps. The recall cites a design defect that can allow backflow from secondary piggyback containers into primary IV lines and prevent priming.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall 36,936 Units for Backflow and Occlusion Risk (2025)

B Braun Medical Inc. recalls 36,936 IV administration sets used with Infusomat Space and other pumps worldwide. The recall was announced Oct. 29, 2025 and includes US and international distribution to Canada, Germany, Guatemala and Singapore. The devices may allow backflow of medication from secondary containers into the primary container and cannot be primed. Stop using immediately and follow the

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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall 122,232 Units Over Backflow Risk (2025)

B. Braun Medical recalled 122,232 IV administration sets sold worldwide through multiple medical distributors. The devices have a backflow risk from secondary (piggyback) IV containers into primary IV containers and may fail to prime. Hospitals and clinics should stop using the sets 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 66,792 Units for Backflow Risk (2025)

B. Braun Medical recalled 66,792 IV Administration Sets sold worldwide through multiple healthcare distributors after reports of backflow and priming occlusion risk. The devices labeled catalog numbers 490241, 490298, and 490360 may allow medication to backflow from piggyback containers into primary lines and may fail to prime. Hospitals and clinicians should stop using immediately and follow the厂

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 3,120 IV Administration Sets for Infusomat Pumps in 2025

B. Braun Medical recalled 3,120 IV administration sets distributed worldwide to hospitals and clinics. The recall concerns potential backflow of medication from secondary piggyback containers into primary containers and an inability to prime. Hospitals and clinicians should stop using the devices immediately and follow the recall instructions issued by the manufacturer.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Blood Administration Set Recall 2025 for 24,624 Units Worldwide

B Braun Medical recalled 24,624 Blood Administration Sets worldwide. The recall covers sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The risk involves backflow from secondary IV containers into primary containers and the inability to prime. Hospitals and clinics should stop using the devices immediately and follow recall instructions.

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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Blood Administration Set Recall 7,344 Units Over Backflow Risk (2025)

B. Braun Medical recalled 7,344 Blood Administration Sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The devices may allow backflow from secondary (piggyback) IV containers into primary IV containers and cannot be primed. Hospitals and healthcare providers should stop using the devices immediately and follow manufacturer instructions.

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Health & Personal Care
HIGH
FDA DEVICE

BBraun Medical Blood Administration Set Recall 5,448 Units (2025)

BBraun Medical recalled 5,448 Blood Administration Sets used with Infusomat Space pumps worldwide sold to hospitals. The recall cites potential backflow of medication from secondary piggyback IV containers into primary IV containers and an inability to prime. Healthcare facilities should stop using the sets immediately and follow recall instructions from B. Braun Medical.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 12,700 ADDitIV Gravity IV Sets Over Backflow Risk (2025)

BBraun Medical recalled 12,700 ADDitIV gravity IV sets distributed worldwide. The sets can backflow medication from piggyback containers into primary IV containers and cannot be primed. Healthcare providers and patients should stop using the sets immediately and follow the recall instructions from BBraun Medical.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recalls 100 V1782F IV Sets Over Backflow Risk (2025)

B Braun Medical Inc. recalled 100 units of the V1782F Univ IV Set W/0.2 MICRON FILTER, distributed worldwide including the US, Canada, Germany, Guatemala, and Singapore. The sets may allow backflow from secondary piggyback IV containers into primary IV containers and cannot be primed. Healthcare facilities should stop using the devices immediately and follow the recall instructions.

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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Outlook IV Set 354214 Recalled for Backflow Risk (2025)

B. Braun Medical recalled the Outlook IV Set 15DR W/2 CARESITE FILTER (Catalog 354214) used with Infusomat Space pumps and BBMI devices. The recall cites backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions by mail.

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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

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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 490238 Extension Set Recalled for IV Backflow Risk (2025)

B. Braun Medical's 490238 Extension Set, used with Infusomat Space Large Volume Pumps and other BBMI devices, is recalled worldwide to hospitals and clinics. The device can allow backflow from secondary piggyback IV containers into the primary container and cannot be primed. Healthcare facilities should stop using the device immediately and follow the manufacturer's recall instructions.

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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 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

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Brand Statistics

Total Recalls
94
Pages
5

Related Brands

B Braun MedicalB BRAUN MEDICAL