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Recalls

A list of FDA Recalls that is updated daily. It references medical equipment and medical product notifications and recalls.

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481 topics in this forum

  1. Heart Pump Recall: Abiomed, Inc. Updates Use Instructions for Impella RP with SmartAssist and Impella RP Flex with SmartAssist Due to A Risk That the Tip of Guidewires or Other Medical Devices May Come into Contact with The Impella Pump During Insertion,

    By FDA Recalls,
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    • 427 views

  3. ICU Medical Issues Nationwide Recall of Potassium Chloride Injection, 20 mEq and Potassium Chloride Injection, 10 mEq Due to Mislabeling

    By FDA Recalls,
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    • 364 views

  4. Breathing Circuit Kit Recall: Sentec/Percussionaire Removes VDR4 Phasitron Breathing Circuits due to Venturi Component Malfunctions that May Reduce Pressure and Volume Flow

    By FDA Recalls,
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    • 306 views

  5. Early Alert: Atherectomy Catheter System Issue from Bard Peripheral Vascular

    By FDA Recalls,
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    • 397 views

  6. Arterial Catheter Recall: Medline Industries, LP, Removes Integrated Arterial Catheters due to Excess Material at Catheter Hub that May Detach

    By FDA Recalls,
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    • 396 views

  7. Continuous Ventilator Correction: Baxter Healthcare Corporation Issues Correction for Life2000 Ventilator due to a nonconforming battery charger, which triggers a battery alarm and renders the ventilator inoperable

    By FDA Recalls,
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    • 399 views

  8. FDA Alerts Patients to Regularly Check Diabetes-Related Smartphone Device Alert Settings, Especially Following Phone Hardware or Software Changes

    By FDA Recalls,
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    • 329 views

  9. Oxygen Concentrator Recall: JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD Removes JMC5A Ni/TruAire-5 Oxygen Concentrator due to the devices spontaneously catching fire

    By FDA Recalls,
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    • 365 views

  10. Pressure Monitoring Device Recall: Medtronic Neurosurgery Issues Correction for Becker and Exacta External Drainage and Monitoring Systems Due to Cracks And/Or Leaks in Stopcocks

    By FDA Recalls,
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    • 389 views

  11. Alvogen Issues Voluntary Nationwide Recall for One Lot of Fentanyl Transdermal System 25 mcg/h Due to a Defective Delivery System

    By FDA Recalls,
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    • 485 views

  12. Update on Alert: Endoscope Accessories Forceps/Irrigation Plug Issue from Olympus

    By FDA Recalls,
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    • 402 views

  13. Update on Alert: Infusion Pump Issue from Fresenius Kabi USA

    By FDA Recalls,
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    • 442 views

  14. Gas Powered Emergency Resuscitator Recall: Mercury Medical Removes Neo-Tee T-Piece Resuscitator Due to An Undersized Spring in The Controller That May Prevent the Device from Delivering the Required Pressure Levels Needed for Effective Ventilation

    By FDA Recalls,
    • 0 replies
    • 299 views

  15. Update on Alert: Nephroscope Sheath Issue from Trokamed GmbH

    By FDA Recalls,
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    • 405 views

  16. Update on Alert: Fluid Delivery Set Issue from Medline

    By FDA Recalls,
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    • 373 views

  17. Update on Alert: Extracorporeal Blood Circuit Issue from Nuwellis

    By FDA Recalls,
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    • 351 views

  18. Cybersecurity Vulnerabilities with Certain Patient Monitors from Contec and Epsimed: FDA Safety Communication

    By FDA Recalls,
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    • 347 views

  19. Olympus Issues Medical Device Advisory Notice to Use Alternative Devices to the MAJ-891 Forceps/Irrigation Plug

    By FDA Recalls,
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    • 347 views

  20. Glucose and Glucose/Ketone Meter Correction: Nova Biomedical Corporation Issues Software Correction for StatStrip Glucose and Glucose/Ketone Hospital Meters Due to Risk for Transmission of Incorrect Patient Results

    By FDA Recalls,
    • 0 replies
    • 305 views

  21. Provepharm Inc. Issues Voluntary Nationwide Recall of One Lot of Phenylephrine Hydrochloride Injection, USP, 10 mg/ mL (Pharmacy Bulk Package) Due to Presence of Particulate Matter

    By FDA Recalls,
    • 0 replies
    • 332 views

  22. Copaxone, Glatopa (glatiramer acetate): Drug Safety Communication - FDA Adds Boxed Warning About a Rare but Serious Allergic Reaction Called Anaphylaxis

    By FDA Recalls,
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    • 383 views

  23. Max Mobility / Permobil Issues Nationwide Recall of SmartDrive Speed Control Dial Due to the Motor Being Unresponsive to the User

    By FDA Recalls,
    • 0 replies
    • 489 views

  24. почивка в Гран Канария

    By pochivka_klon,
    • 0 replies
    • 323 views

  25. Early Alert: Solution Set Issue from Baxter Healthcare Corporation

    By FDA Recalls,
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    • 514 views

  26. Early Alert: Fluid Delivery Set Issue from Medline

    By FDA Recalls,
    • 0 replies
    • 419 views
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