stop use immediately Recalls

2,153 recalls tagged with “stop use immediately”.

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.

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
Potential for
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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 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
Potential for
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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

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.

B Braun Medical
Potential for
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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
Potential for
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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
Potential for
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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
Potential for
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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
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Medicrea Recalls Implant Inserter Over Rotation Failure Risk

Medicrea recalled 44 units of its IB3D Universal Implant Inserter on October 29, 2025. The device's handle may untread from the shaft, preventing proper rotation of implants. The recall affects states including TN, CA, and TX.

Medicrea
Due to
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall: 5,100 Units Distributed Worldwide Over Backflow and Oc

B Braun Medical Inc. recalls 5,100 IV administration sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The recall cites backflow of medication from piggyback containers into primary IV containers and an occlusion that prevents priming. Patients should stop use immediately and follow recall instructions.

BB Braun Medical
Potential for
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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
Potential for
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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
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 12,320 IV Burette Sets Over Backflow Risk (2025)

B. Braun Medical Inc. is recalling 12,320 burette sets worldwide used with Infusomat Space, Outlook Pump, and Vista Basic Pump. The device can allow backflow from secondary IV containers into primary containers and may fail to prime. Hospitals and clinics should stop using the device immediately and follow the recall instructions.

B. Braun Medical
Potential for
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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
Potential for
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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
Potential for
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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
Potential for
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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

B Braun Medical
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Tag Statistics

Total Recalls
2,153

Related Tags

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