Drugs & medicalClass II

Breas Medical, Inc. recalls Vivo 45LS Ventilator- intended to provide continuous or intermittent ventilatory support for the care of individuals who require…

A forced shutdown of one of the processors did not generate a watch dog alarm, would develop into a failure AND the instructions to monitor a ventilator dependent patient are NOT followed, the health consequences could…

Read the official notice →
Date
2022-07-20
Country
United States
Brand
Breas Medical
Product
Vivo 45LS Ventilator- intended to provide continuous or intermittent ventilatory support for the care of individuals who require…
Classification
Class II
Units
Nationwide
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Breas Medical recalls

  1. 2024-09-11
  2. US
    Drugs & medicalClass I

    Breas Medical, Inc. recalls Vivo 45 LS, pressure and volume ventilator capable of delivering continuous or intermittent ventilatory support for patients who require…

    There is a potential for short term (<7 days) elevated levels of formaldehyde emitted from the device into the patient breathing airpath in specific conditions.

    FDA · DeviceBreas Medical, Inc.US Nationwide.Official notice →
  3. 2023-12-06
  4. US
    Drugs & medicalClass II

    Breas Medical, Inc. recalls with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits: 006093, 006653, an accessory to ventilator device, Vivo 45LS.…

    Produced with unintended open slits on the side of the mouthpiece body, may result in insufficient ventilation in spontaneous breathing patients using MPV-VCV and MPV-PCV modes of ventilation

    FDA · DeviceBreas Medical, Inc.Nationwide Foreign: CanadaOfficial notice →
  5. 2022-04-20
  6. US
    Drugs & medicalClass II

    Breas Medical, Inc. recalls Breas Ventilator Trolley with the Vivo 50/60/65 and Vivo 45LS ventilator models Article no 007384

    Ventilator mounting brackets for the Vivo 50/60/65 and Vivo 45LS ventilator models can become detached from the Breas Ventilator Trolley, this may cause the ventilator to fall from the trolley and cause injury to a…

    FDA · DeviceBreas Medical, Inc.US NationwideOfficial notice →
All 4 Breas Medical recalls →

Other drugs & medical recalls in the United States

  1. 2022-07-20
  2. US
    Drugs & medicalClass III

    Hamilton Medical AG recalls HAMILTON-H900 Humidifier, Models: 950001, 950004

    When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm…

    FDA · DeviceHamilton Medical AGUS: WI, FL, CA, NV, PA, TX, PAOfficial notice →
  3. US
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    Agilent Technologies, Inc. recalls Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF K589911-2 Anti-FITC-AP CISH Accessory Kit (Dako Omnis), Box A REF…

    Label provided for substrate vail contained incorrect expiration date.

    FDA · DeviceAgilent Technologies, Inc.U.S. Nationwide distribution in the states of NY and VA.Official notice →
  4. US
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    Aesculap Implant Systems LLC recalls AESCULAP TC COOELY MICRO NEEDLEHLDER SERR 200MM, product code MG524R. manual surgical instrument designed to grasp a suture needle

    Needleholder incorrectly labeled as 200MM when the actual instrument size is 150MM.

    FDA · DeviceAesculap Implant Systems LLCUnited States: TX and AKOfficial notice →
  5. US
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    Ivenix, Inc. recalls Ivenix Infusion System (IIS)

    Downstream occlusion alarm is sometimes immediately followed by a pump problem alarm.

    FDA · DeviceIvenix, Inc.US Nationwide distribution in the states of NJ and WI.Official notice →
  6. US
    Drugs & medicalClass II

    Waldemar Link GmbH & Co. KG (Mfg Site) recalls Tibial Component Modular. orthopedic prosthesis. Model Nos: Small, W 16-2817/32 Medium, W 16-2817/35 Large, W 16-2817/37

    There is a risk that blind screws of the modular tibial component cannot be loosened intraoperatively. This may lead to prolongation of surgery due to an intraoperative change in procedure.

    FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)Domestic distribution to AL, CA, FL, GA, IL, IN, KS, MI, MN, NV, NY, OH, TN,…Official notice →
  7. US
    Drugs & medicalClass II

    DePuy Orthopaedics, Inc. recalls MODULAR CATHCART FRACTURE HEAD HIP BALL, sizes 41mm to 60mm inclusive; metallic femoral head prosthesis, Product No. 136341000,…

    The Cathcart Ball has an inherent +5mm offset which is not currently specified in its Instructions for Use or Surgical Technique Guide. The STG has been updated to reflect the clarification that the +5mm offset should…

    FDA · DeviceDePuy Orthopaedics, Inc.Worldwide distribution - US Nationwide and the countries of Australia,…Official notice →
See all drugs & medical recalls →