All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall 2025 Affects 6,768 Units Over Backflow Risk

6,768 IV administration sets are recalled worldwide by B Braun Medical. The recall covers devices used with gravity and pump systems. The hazard is potential backflow of medication into primary IV containers and inability to prime. Stop using the product and follow the recall instructions immediately. Contact B Braun Medical for instructions via the FDA recall page linked below.

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.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall Affects 286,400 Units Across Global Pumps (2025)

B. Braun Medical recalls 286,400 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump worldwide. The devices may backflow from secondary IV containers into primary containers and cannot be primed. Stop using the device immediately and follow recall instructions from the manufacturer.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recall 2025 Affects 5,900 Units Over Backflow Risk

B. Braun Medical Inc recalled 5,900 IV administration sets worldwide, including the United States, after reports of backflow from piggyback to primary IV containers and potential priming failure. The devices are used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Hospitals and clinics should stop using the sets and follow manufacturer recall instructions.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Outlook IV Set Recall 18,072 Units for Backflow Risk (2025)

B. Braun Medical Inc. recalled 18,072 Outlook IV Sets used with the Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The devices pose a risk of backflow of medication from secondary IV containers into the primary and an occlusion that can prevent priming. Healthcare providers and patients should stop using the device immediately and follow recall instructions sent by mail.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recalls 18,984 IV Administration Sets Over Backflow Hazard

B Braun Medical recalled 18,984 IV administration sets after discovering a potential for backflow of medication from secondary IV containers into primary containers. This defect creates a high risk of medication errors and occlusion. Patients and healthcare providers should stop using these sets immediately and contact B Braun Medical for further instructions.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall Affects 2,544 Units Worldwide

B Braun Medical Inc recalled 2,544 IV administration sets due to risk of backflow from secondary piggyback containers into primary IV lines and inability to prime. The recall covers products used with BBMI Infusomat Space, Outlook, and Vista Basic pumps and distributed worldwide including the US, Canada, Germany, Guatemala and Singapore. Patients should stop using the device immediately and follow

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 554,015 SafeDAY IV Sets Over Backflow Risk (2025)

B. Braun Medical recalled 554,015 SafeDAY IV administration sets distributed worldwide on Oct 29, 2025. The devices can backflow medication from secondary piggyback containers into primary IV containers and may fail to prime. Hospitals and clinics should stop using the affected sets and follow the manufacturer’s recall instructions.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

BBMIs Infusomat IV Administration Set Recall, 63,192 Units Worldwide for Backflow and Occlusion Risk

BBMI recalled 63,192 IV administration sets worldwide on Oct 29, 2025. The recall affects the IV administration set labeled as 490426 with UDIs listed. The defect is potential backflow from secondary to primary IV containers and an inability to prime. Patients and healthcare providers should stop using these devices immediately and follow the manufacturer’s recall instructions.

BB 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.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Sets Recall Over Backflow and Occlusion Risk (2025)

B Braun Medical Inc. recalls 190,625 IV administration sets worldwide, including US and Canada, for risk of backflow from secondary to primary IV containers and occlusion that prevents priming. The recall affects BBMI’s Infusomat Space, Outlook Pump, and Vista Basic Pump compatible sets. Stop-use immediately and follow recall instructions.

BBraun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for Backflow and Occlusion Risk (2025)

B Braun Medical Inc recalled 1,019 IV administration sets worldwide after reports of backflow and occlusion. The devices were used with BBMI Infusomat Space, Outlook, and Vista Basic pumps. The recall affects a single catalog number 457506 with UDI details. Patients should stop using the device and follow manufacturer instructions for return.

BBraun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Sets Recalled for Backflow Risk and Occlusion (2025)

B Braun Medical Inc. recalls 111,312 IV Administration Sets worldwide, including US and international markets, due to backflow risk and occlusion. The recall affects catalog numbers 490193 and 490326, used with Infusomat Space, Outlook, and Vista Basic pumps. Stop using immediately and follow recall instructions for refunds or replacements.

B Braun Medical
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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.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

BBraun Medical IV Administration Set Recalled for Backflow and Occlusion Risk (490491, 2025)

BBraun Medical Inc recalls 960 IV administration sets distributed worldwide due to backflow risk and inability to prime. The recall affects the IV administration set catalog number 490491 with UDI-DI 04046955086931. The device can allow medication to flow from secondary piggyback containers into primary IV containers and may not prime properly. Stop using immediately and follow recall instructions

BBraun Medical
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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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