Health & Personal Care Recalls

1,882 product recalls found in this category. Browse through all safety alerts and stay informed.

High Activity Category

This category has a significant number of recalls. Please check regularly for updates.

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

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 FOOD

Avion Pharmaceuticals Prenate Chewable Prenatal Vitamin Recalled for Undeclared Soy (804 Bottles, 5

Avion Pharmaceuticals recalled 804 bottles of Prenate Chewable prenatal vitamins shipped to 17 states after tests found undeclared soy and a boron labeling error. The product lists boron as 250 mg per serving instead of 250 mcg per serving. Consumers should not take the product and should contact Avion Pharmaceuticals for refund or replacement.

Avion Pharmaceuticals
Undeclared Soy.
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical ADDitIV Sets Recalled for High Backflow and Occlusion Risk, 43,900 Units Worldwide

B Braun Medical Inc. recalls 43,900 ADDitIV gravity and pump administration sets. The recall covers catalog numbers V1443, V1447, V1448, and V1484. The issue is backflow of medication from secondary IV containers into primary containers and inability to prime the line. Patients and healthcare providers should stop using these devices immediately and follow recall instructions.

B Braun Medical
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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.

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 Sets Recalled for Backflow and Occlusion Risk (490549, 490565)

B. Braun Medical Inc. is recalling 65,232 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump worldwide. The devices pose a risk of backflow from secondary piggyback IV containers into primary IV containers and may fail to prime due to occlusion. Hospitals and healthcare providers should stop using the affected sets immediately and follow the maker

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 15,250 PB1500 IV Set Over Backflow Risk (2025)

B. Braun Medical recalled 15,250 PB1500 15-DROP IV SETS distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. The devices pose a backflow risk from secondary IV containers into primary containers and may fail to prime. Healthcare facilities should stop using the product and follow recall instructions.

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

B Braun Medical Recalls 19,104 IV Administration Sets for Backflow Risk (2025)

B Braun Medical recalls 19,104 IV Administration Sets distributed worldwide, including the United States and international distribution to Canada, Germany, Guatemala, and Singapore. The recall cites backflow of medication from secondary piggyback IV containers into primary IV lines and an inability to prime due to occlusion. The affected catalog number is 490400. Stop using the device and follow a

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

B. Braun Medical IV Administration Set Recall for 29,900 Units Over Backflow and Occlusion Risk (202

B. Braun Medical recalled 29,900 IV administration sets distributed worldwide through medical distributors. The recall is linked to backflow from secondary to primary IV containers and an inability to prime. Healthcare providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.

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

B. Braun Medical IV Administration Sets Recalled for Backflow Risk — 1,861,111 Units (2025 Recall)

B. Braun Medical recalled 1,861,111 IV Administration Sets sold globally through hospitals and medical distributors. The sets may allow backflow from secondary to primary IV containers and cannot be primed. Hospitals and clinicians using these sets with Infusomat Space, Outlook, or Vista Basic Pumps should stop using them immediately and contact B. Braun Medical for instructions.

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

B. Braun Medical IV Administration Set Recall 2025 for Backflow and Occlusion Risk (490437)

B. Braun Medical recalled 4,536 IV administration sets globally after reports of backflow risk and occlusion. The sets labeled catalog 490437 are used with gravity IV administration and pump systems such as Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Patients and healthcare providers 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 Inc. IV Administration Set Recalled for Backflow and Priming Occlusion (490407)

B Braun Medical Inc. recalled 10,896 IV administration sets globally due to backflow risk and occlusion. The recall covers the IV ADMIN SET W/ CARESITE EXT SET with Catalog Number 490407 used with BBMI pumps. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.

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

B. Braun Medical Recalls 9,500 IV Administration Sets for Backflow and Occlusion Risk (2025 Recall)

B. Braun Medical Inc. recalled 9,500 IV administration sets with worldwide distribution including the United States, Canada, Germany, Guatemala and Singapore. The devices may backflow medication from secondary piggyback IV containers into primary IV containers and may fail to prime. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer's recall’s,[

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

B. Braun Medical IV Administration Set Recalled for 126,050 Units Over Backflow Risk (2025)

B. Braun Medical recalled 126,050 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The recall cites potential backflow from secondary to primary IV containers and an inability to prime. Health care providers and patients should stop using the device immediately and follow recall instructions from the manufacturer.

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

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

B Braun Medical Inc. recalls 168,816 IV administration sets worldwide, including US and international distributors. The recall targets gravity and pump administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The issue is potential backflow from piggyback containers into primary IV containers and inability to prime.

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

B. Braun Medical Recalls 48-Unit IV Administration Set for Backflow Risk (2025)

B. Braun Medical recalled 48 IV Administration Sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The devices carry a backflow and occlusion risk between secondary and primary IV containers. Healthcare providers and patients should stop using immediately and follow recall instructions. A recall letter will provide further guidance on returning or replacing the 제품

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

B. Braun Medical IV Administration Set Recall for 129,480 Units in 2025

B. Braun Medical recalled 129,480 IV Administration Sets sold worldwide to hospitals and clinics. The devices can backflow from secondary piggyback IV containers into primary containers and cannot be primed, risking incorrect dosing. Hospitals and healthcare providers should stop using the devices immediately and follow the recall instructions from B. Braun Medical.

B. Braun Medical
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Category Statistics

Total Recalls
1,882
Pages
95