Drug Recalls Center

1,894 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.

1,894
Total Drug Recalls
24
High Risk Medications
FDA
Official Source

Important Medication Safety Information

  • Do not stop taking prescribed medications without consulting your healthcare provider
  • Contact your pharmacist or doctor if you have a recalled medication
  • Check lot numbers carefully - not all batches may be affected
  • Return recalled medications to your pharmacy for proper disposal

Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.

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
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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
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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 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 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
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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
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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
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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
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Philips CT Scanner Recalled Over Potential Detachment Hazard

Philips North America recalled six units of the Incisive CT scanner on October 29, 2025, due to a serious safety hazard. The screws on the tube heat exchanger may not be properly tightened, leading to potential detachment during operation. This defect could cause damage to other components within the system.

Philips North America
If the
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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 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
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 Inc. Recalls 28,344 IV Administration Sets Linked to Backflow and Occlusion Risks (Z

B Braun Medical Inc. recalls 28,344 IV administration sets used with several BBMI infusion pumps after reports of backflow and occlusion risks. The recall covers a catalog number 470179 device distributed worldwide including the U.S., Canada, Germany, Guatemala and Singapore. The issue involves potential backflow from secondary IV containers into primary containers and the inability to prime the管.

BBraun Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical IV Administration Set Recall 23,160 Units for Backflow Risk in 2025

BBraun Medical recalled 23,160 IV administration sets distributed worldwide, including the US and Canada, after reports of backflow and occlusion risk. The recall involves catalog number 490487 and UDIs 04046955086856 and 04046955086849. Stop using the product immediately and follow manufacturer instructions for recall procedures.

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

B. Braun Medical Recalled 19,320 Anesthesia IV Sets for Backflow Risk (2025)

B. Braun Medical Inc. recalled 19,320 Anesthesia IV Sets used with Infusomat Space Large Volume Pumps and related BBMI devices sold worldwide through healthcare facilities. The devices pose a backflow risk from secondary piggyback IV containers into the primary IV container and cannot be primed. Healthcare facilities and patients should stop using the device immediately and follow the manufacturer

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

B. Braun Medical Anesthesia IV Set Recall for Backflow Risk in 2025 (58,752 Units)

B. Braun Medical recalled 58,752 Anesthesia IV Sets used with Infusomat Space pumps and other BBMI devices. The recall targets backflow from secondary piggyback IV containers to primary containers and occlusion. Hospitals and clinicians should stop using the device immediately and await manufacturer guidance by recall letter.

B Braun Medical
Potential for
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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 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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