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 490245 Recalled for Backflow Risk (2025)

B. Braun Medical Inc. recalls 40,992 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps sold to hospitals worldwide. The recall targets the IV administration set catalog number 490245. The defect is backflow of medication from secondary piggyback containers into primary containers and an inability to prime. Healthcare providers and patients should stop using theDevice

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 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

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 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

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 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

B Braun Medical IV Administration Set Recall for 4,488 Units in 2025

B Braun Medical recalled 4,488 IV administration sets distributed worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices risk backflow from secondary (piggyback) IV containers into primary containers and may be unable to prime due to occlusion. Healthcare facilities and patients should stop using immediately and follow recall instructions from the maker.

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

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

B. Braun Medical Inc. IV Administration Set Recall for 1,080 Units in 2025 recall

B. Braun Medical Inc. recalls 1,080 IV Administration Sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall addresses backflow from secondary piggyback containers into primary IV containers and an inability to prime (occlusion). Health care providers and patients should stop using the devices immediately and follow the manufacturer’s recall instructions.

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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 31,392 IV Administration Sets for Backflow Risk (2025)

B. Braun Medical Inc. recalls 31,392 IV administration sets used with Infusomat Space and other pumps worldwide. The device may allow backflow from piggyback containers into primary IV lines and cannot be primed. Hospitals 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 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

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 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 Recall for Backflow Risk (490566) 2025

B Braun Medical recalled its IV Administration Set used with Infusomat Space Large Volume Pumps and related models. The recall cites backflow of medication from secondary to primary IV containers and an occlusion that prevents priming. Hospitals and clinicians should stop using the device immediately and follow manufacturer recall instructions.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical 490202 Extension Set Recall: 13,600 Units Over Backflow Risk (2025)

B Braun Medical Inc recalled 13,600 extension set units used with Infusomat Space and related pumps sold through multiple healthcare distributors worldwide. The recall cites a backflow risk from secondary piggyback containers into primary IV containers and an inability to prime due to occlusion. Healthcare providers and facilities should stop using the device immediately and follow manufacturer-re

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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Infusion Extension Set Recall for 11,650 Units Over Backflow Risk (2025)

B. Braun Medical recalls 11,650 extension sets used with Infusomat Space pumps sold worldwide after a backflow and priming defect. The device can allow medication to flow from a piggyback container into the primary line and may not prime properly. Hospitals and patients should stop using the device immediately and follow recall instructions from the manufacturer.

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