Health & Personal Care Recalls

1,814 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 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
Potential for
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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
Potential for
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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
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Outlook IV Set Recall 162,648 Units for Backflow Risk (2025)

B Braun Medical recalled 162,648 Outlook IV Sets used with Infusomat Space Large Volume Pumps and related systems. The devices carry a backflow risk from secondary piggyback IV containers into primary IV containers and may fail to prime. Hospitals and patients 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 Vista IV Set Recall for 74,652 Units Over Backflow and Occlusion Risk

B Braun Medical Inc recalls 74,652 Vista IV sets used with Infusomat Space and Vista Basic Pumps due to backflow and occlusion risks. The recall affects devices distributed worldwide, including the US, Canada, Germany, Guatemala, and Singapore. Stop using the device immediately and follow manufacturer instructions.

BBraun 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 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
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical SAFELINE IV Sets Recalled for 46,250 Units Over Backflow Risk (2025)

B. Braun Medical recalled 46,250 SAFELINE IV sets sold worldwide on Oct. 29, 2025. The devices pose a backflow risk from secondary piggyback IV containers into primary lines and may fail to prime due to occlusion. Hospitals and patients using Infusomat Space Large Volume Pump, Outlook Pump, or Vista Basic Pump with SAFELINE sets should stop use immediately and await manufacturer instructions.

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

B Braun Medical IV Administration Set Recall 11,832 Units Over Backflow Risk (2025)

B Braun Medical recalled 11,832 IV administration sets worldwide on Oct 29, 2025. The devices are used with Infusomat Space, Outlook, and Vista Basic Pumps. The hazard is backflow of medication and occlusion. Stop using the product immediately and follow manufacturer recall instructions. Check your model numbers and contact the manufacturer for refunds or replacements.

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

B. Braun Medical IV Administration Set Recall for 187,464 Units Over Backflow Risk (2025)

B. Braun Medical recalled 187,464 IV administration sets worldwide, including US distribution and shipments to Canada, Germany, Guatemala, and Singapore. The devices pose a backflow risk from secondary (piggyback) IV containers into primary containers and can fail to prime properly. Healthcare providers and patients 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

B. Braun Medical Rate Flow IV Set Recalled for 150,664 Units in 2025

B. Braun Medical recalled 150,664 Rate Flow IV Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The devices are cataloged as 375258. The recall addresses a potential backflow from piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s rec

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

Baxter Healthcare Recalls Blood Pressure Cuff Replacement Bladder

Baxter Healthcare recalled 118 units of the Welch Allyn INF BAG, Model REF 5089-18, on October 28, 2025. The replacement bladder may contain a Large Adult size bladder instead of a Thigh size bladder. This defect poses a high risk for inaccurate blood pressure readings.

Baxter Healthcare
Replacement bladder
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Health & Personal Care
HIGH
FDA DRUG

Agebox iKids-Growth Recalled Over Undeclared Ibutamoren

Agebox recalled its iKids-Growth Night Formula due to the presence of undeclared ibutamoren. The recall affects 60-count bottles manufactured exclusively for AGEBOX Inc. Consumers should stop using the product immediately and contact Agebox or their healthcare provider for guidance.

Agebox
Marketed Without
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Health & Personal Care
HIGH
FDA DEVICE

Illumina NextSeq 550Dx Reagent Kits Recalled for Leaky Flow Cells Affecting 11,916 Units Worldwide

Illumina recalled 11,916 NextSeq 550Dx reagent kits and flow cells worldwide after identifying a gasket defect that can leak during sequencing. The issue may cause run failures, no or insufficient data output, instrument fluidics clogs and potential exposure to toxic substances. Healthcare providers and users should stop using the affected kits and await recall instructions from Illumina.

Illumina
An instrument
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Health & Personal Care
HIGH
FDA DRUG

Agebox iKids-Growth Capsules Recalled Over Undeclared Ingredient

AGEBOX Inc. recalled 665 bottles of iKids-Growth capsules on October 28, 2025, due to undeclared ibutamoren. The product was marketed without an approved NDA/ANDA. Consumers should stop using the product immediately and contact Agebox for guidance.

Agebox
Marketed Without
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Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls Azurion 7 M20 X-ray System Over Safety Concern

Philips North America recalled 110 Azurion 7 M20 interventional fluoroscopic X-ray systems on October 27, 2025. These devices were shipped without the necessary Source-to-Skin Distance (SSD) Spacer, violating FDA regulations. The absence of this spacer poses a serious health risk during fluoroscopy applications.

Philips North America
Between July
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Health & Personal Care
HIGH
FDA DEVICE

Nipro Medical Hemodialysis System Recalled Due to Screw Hazard

Nipro Medical Corporation recalled the Surdial DX Hemodialysis System on October 27, 2025, after reports of screws loosening and potentially falling out. The recall affects devices distributed nationwide across 19 states. Patients and healthcare providers must stop using the device immediately and follow manufacturer guidance.

Nipro Medical
Screw may
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Adhesive Bandages Due to Sterility Concerns

Medline recalled 4.4 million Quick Strip Plastic Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals compromising sterility. Consumers and healthcare providers should stop using these bandages immediately.

Medline Industries, LP
Medline has
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Category Statistics

Total Recalls
1,814
Pages
91