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 Set Recall Affects 32,436 Units Over Backflow and Occlusion Risks (2025)

B Braun Medical Inc. recalled 32,436 Anesthesia IV Sets used with Infusomat Space, Outlook Pump, and Vista Basic Pump after reports of backflow risk and occlusion. The recall covers catalog numbers 490189 and 490226 distributed worldwide, including the US, Canada, Germany, Guatemala and Singapore. Consumers should stop using the device immediately and follow manufacturer instructions for recall. A

BBraun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Anesthesia IV Set Recalled for Backflow Risk (10,536 Units) 2025

B. Braun Medical recalled 10,536 Anesthesia IV Sets sold through multiple retailers worldwide after a potential backflow from piggyback to primary IV lines and occlusion. The devices are used with Infusomat Space Large Volume Pumps, Outlook Pumps, and Vista Basic Pumps. Hospitals and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Infusomat IV Sets Recalled for Backflow and Occlusion Risk (49,330,370 Units)

B. Braun Medical recalled 49,330,370 Infusomat IV sets worldwide after a potential backflow from secondary to primary IV containers and an inability to prime. The recall covers gravity IV sets and pump sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. Stop using any affected sets immediately and contact B. Braun Medical for instructions on refunds or replacement

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

BBraun Medical Inc. Recalled 104,784 Anesthesia IV Sets Over Backflow, Occlusion Risk

BBraun Medical Inc. recalled 104,784 Anesthesia IV Sets used with Infusomat Space, Outlook, and Vista Basic pumps. The recall cites backflow of medication from secondary to primary IV containers and a potential inability to prime. Health care providers should stop using the devices immediately and follow the manufacturer’s recall instructions for refund or replacement.

BBraun 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
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical 490202 Extension Set Recall: 13,600 Units Over Backflow Risk (2025)

B Braun Medical Inc recalled 13,600 extension set units used with Infusomat Space and related pumps sold through multiple healthcare distributors worldwide. The recall cites a backflow risk from secondary piggyback containers into primary IV containers and an inability to prime due to occlusion. Healthcare providers and facilities should stop using the device immediately and follow manufacturer-re

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B Braun Medical Extension Set Recalled for 1,200 Units Over Backflow and Occlusion Risk (2025 Recall

B Braun Medical recalled 1,200 extension sets used with Infusomat Space large-volume pumps distributed worldwide to hospitals and clinics. The recall cites potential backflow from secondary IV containers into primary containers and an inability to prime (occlusion). Healthcare facilities should stop using the devices immediately and follow the recall instructions issued by the manufacturer.

B Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Blood Administration Set Recall 33,528 Units for Backflow Risk (2025)

B. Braun Medical recalled 33,528 Blood Administration Set units used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump. The sets have a backflow risk from secondary piggyback IV containers into primary IV containers and may fail to prime. Health-care facilities should stop using the device immediately and follow the recall letter instructions.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical Recalls 32,500 Caresite Extension Sets for IV Pumps (2025)

B. Braun Medical recalled 32,500 Caresite Extension Sets used with Infusomat Space, Outlook, and Vista Basic IV pumps worldwide. The devices pose a backflow and occlusion risk in the primary IV line. Hospitals and healthcare providers should stop using the device immediately and follow the recall instructions.

B. Braun Medical
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Extension Set Recall 2,100 Units Over Backflow Risk (2025)

B. Braun Medical Inc. recalled 2,100 IV Extension Sets used with Infusomat Space, Outlook and Vista Basic pumps sold worldwide to healthcare facilities. The extension set presents a backflow risk from secondary to primary IV containers and can hinder priming. Hospitals and clinicians should stop using the device immediately and follow the recall instructions provided by the manufacturer.

B. Braun Medical
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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
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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
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical IV Administration Set Recalled for Backflow Risk in 65,904 Units (2025)

B. Braun Medical recalled 65,904 IV Administration Sets used with Infusomat Space Large Volume Pump, Outlook Pump and Vista Basic Pump. The recall cites backflow of medication from secondary (piggyback) IV containers into primary containers and an inability to prime. Hospitals 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 Backflow Risk (2025)

B Braun Medical recalled 135,000 IV administration sets used with Infusomat Space Large Volume Pump, Outlook Pump, and Vista Basic Pump, sold worldwide to hospitals and other healthcare providers. The devices pose a backflow risk from secondary to primary IV containers and can fail to prime. Health care facilities should stop using the affected sets and follow the manufacturer’s recall guidance.

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

B. Braun Medical Recalls 554,015 SafeDAY IV Sets Over Backflow Risk (2025)

B. Braun Medical recalled 554,015 SafeDAY IV administration sets distributed worldwide on Oct 29, 2025. The devices can backflow medication from secondary piggyback containers into primary IV containers and may fail to prime. Hospitals and clinics should stop using the affected sets and follow the manufacturer’s recall instructions.

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
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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 Outlook IV Set 354214 Recalled for Backflow Risk (2025)

B. Braun Medical recalled the Outlook IV Set 15DR W/2 CARESITE FILTER (Catalog 354214) used with Infusomat Space pumps and BBMI devices. The recall cites backflow from secondary piggyback IV containers into primary containers and an inability to prime. Hospitals and healthcare providers should stop using the device immediately and follow recall instructions by mail.

B. Braun Medical
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