stop use immediately Recalls

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

Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Recalls 98,568 IV Administration Sets for Backflow and Occlusion Risk (2025)

B Braun Medical recalled 98,568 IV administration sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall covers catalog number 490274 and UDI-DI codes. The device presents a backflow risk and inability to prime. Hospitals and patients 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 IV Administration Set Recall for 45,288 Units Over Backflow Risk (2025)

B. Braun Medical has issued an active recall for 45,288 IV administration sets catalog 490412. The devices support gravity and pump-based IV administration with Infusomat Space, Outlook, and Vista Basic Pumps. The recall cites a design defect that can allow backflow from secondary piggyback containers into primary IV lines and prevent priming.

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

B. Braun Medical IV Administration Set Recall for 5,952 Units Over Backflow Risk (2025)

B. Braun Medical Inc. recalled 5,952 IV Administration Sets distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore, for use with Infusomat Space, Outlook, and Vista Basic Pumps. The units carry Catalog Number 490612. The recall cites potential backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare teams

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

B. Braun Medical IV Administration Set Recall 2025 Affects 259,392 Units

B. Braun Medical recalled 259,392 IV administration sets worldwide on Oct. 29, 2025. The devices could allow backflow of medication from secondary (piggyback) IV containers into primary IV containers and may not prime due to occlusion. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions in the notice.

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

B Braun Medical Recalls 12,200 IV Administration Sets for Backflow and Occlusion Risk (2025)

B Braun Medical recalls 12,200 IV administration sets sold to hospitals and medical distributors worldwide. The devices labeled NF1503 and catalog number 490062 may allow backflow of medication from secondary piggyback IV containers into primaries and may fail to prime. Hospitals should stop using the devices 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 Set Recall Affects 41,976 Units Worldwide (2025)

B Braun Medical recalled 41,976 IV Administration Sets sold worldwide after identifying a backflow risk. The device can allow medication to flow from secondary (piggyback) containers into the primary IV line and may not prime properly. Hospitals and healthcare providers should stop using the sets immediately and await recall instructions from B Braun Medical.

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

B. Braun Medical IV Administration Set Recall for 1,250 Units Over Backflow Risk (2025)

B. Braun Medical recalled 1,250 IV administration sets distributed worldwide to hospitals and clinics. The devices may allow backflow of medication from secondary (piggyback) IV containers into primary containers and may not prime properly. Hospitals and other healthcare providers 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 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
Potential for
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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
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall for 41,016 Units Over Backflow and Occlusion Risk (2025

B Braun Medical Inc. recalled 41,016 IV administration sets sold worldwide, including the United States, Canada, Germany, Guatemala and Singapore. The devices pose a risk of backflow from secondary piggyback IV containers into primary containers and may fail to prime. Healthcare providers and patients should stop using the device immediately and follow recall instructions sent by letter.

B Braun Medical
Potential for
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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
Potential for
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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
Potential for
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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
Potential for
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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
Potential for
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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
Potential for
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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
Potential for
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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 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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Tag Statistics

Total Recalls
2,153

Related Tags

fda regulatedimmediate actionreturn for refundreplacement availablecpsc regulatedinfant productadult productsuffocation riskback to schoolelectrical hazardfire hazardburn risk