Drugs & medicalClass II

B. Braun Medical, Inc. recalls AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036

Potential for product leakage from the Spin Lock Connector on the distal end of the device due to the migration of excess solvent during the assembly process.

Read the official notice →
Date
2024-09-25
Country
United States
Brand
B. Braun Medical
Product
AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036
Classification
Class II
Units
US Nationwide distribution.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 B. Braun Medical recalls

  1. 2025-03-26
  2. US
    Drugs & medicalClass II

    B Braun Medical Inc recalls Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged. Passive safety IV catheter.

    Increased risk for valve housing detachment causing leakage.

    FDA · DeviceB Braun Medical IncDomestic: CA, CA, FL, GA, IL, IL, IN, MD, MN, MO, NC, NM, NY, PA, TN, TX, VA,…Official notice →
  3. 2025-02-05
  4. US
    Drugs & medicalClass II

    B. Braun Medical, Inc. recalls Design Options COMBINED SPINAL/EPIDURAL TRAY- Intended for administration of analgesic/anesthetic agent to intrathecal space and epidural…

    Incorrect catheter connector within the kit resulting in inability to provide a secure connection to the epidural catheter. The incorrect catheter connector is smaller than the required catheter connector and therefore…

    FDA · DeviceB. Braun Medical, Inc.US Nationwide distribution in the states of MO, OK.Official notice →
  5. 2024-09-25
  6. US
    Drugs & medicalClass II

    B Braun Medical Inc recalls SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis.…

    Incomplete insertion of the patient connector of the Streamline Airless System Hemodialysis Bloodline to the Locksite may result in the potential for occlusion during prograde rinseback procedures. If the patient…

    FDA · DeviceB Braun Medical IncUS Nationwide distribution.Official notice →
  7. 2024-09-18
  8. US
    Drugs & medicalClass I

    B Braun Medical Inc recalls Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U

    Extension of previous recall RES 92978. Pumps have the potential for upstream occlusion sensor to cease proper function due to buildup of electrostatic charge during operation triggering false downstream and upstream…

    FDA · DeviceB Braun Medical IncUS distribution to AL, CA, GA, IL, MI, and TX.Official notice →
  9. 2024-08-28
  10. US
  11. 2024-07-31
  12. US
    Drugs & medicalClass II

    B Braun Medical Inc recalls Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Wireless Model/Catalog Number: 8713031U Software Version: 8713031U…

    Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with…

    FDA · DeviceB Braun Medical IncDomestic distribution nationwide. International distribution to Canada.Official notice →
All 53 B. Braun Medical recalls →

Other drugs & medical recalls in the United States

  1. 2024-09-25
  2. US
    Drugs & medicalClass II

    Medtronic Inc. recalls 2090 Programmers with serial number prefixes PKK0 and PKK1: a) 2090, Product Description: PRGM 2090 PROGRAMMER-PORTABLE CRM; b) 209031,…

    Medtronic CareLink 2090 programmers with serial number prefixes PKK0 and PKK1 have the potential for autonomous cursor motion when Finger Touchscreen capability is enabled by software version 3.2 or higher.

    FDA · DeviceMedtronic Inc.Worldwide distribution.Official notice →
  3. US
    Drugs & medicalClass II

    Boston Scientific Corporation recalls VTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provide external drainage of the urinary tract.

    There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.

    FDA · DeviceBoston Scientific CorporationUS, Colombia, Philippines, RussiaOfficial notice →
  4. US
    Drugs & medicalClass II

    GE Healthcare GmbH recalls ViewPoint 6, Model Numbers: a) H47581RJ, b) H47591MA, c) H47591MT, d) H47591PE, e) H47591PR, f) H47591RA, g) H47591SD, h) H47591YA;…

    The National Institute of Standards and Technology (NIST) has identified in the National Vulnerability Database (NVD) that NexGen Healthcare Mirth Connect, prior to version 4.4.1, has a potential vulnerability allowing…

    FDA · DeviceGE Healthcare GmbHUS Nationwide distribution including in the states of Alabama, Alaska,…Official notice →
  5. US
    Drugs & medicalClass II

    SEER MEDICAL PTY LTD recalls Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and video EEG (vEEG)…

    During CAPA investigations of sight production inconsistencies, it was highlighted that previous Electromagnetic Compatibility (EMC) assessments related to RF radiated emissions may not be reasonably equivalent to the…

    FDA · DeviceSEER MEDICAL PTY LTDWorldwide - US Nationwide distribution in the states of MN, NY, PA and the…Official notice →
  6. US
    Drugs & medicalClass II

    CareFusion 303, Inc. recalls Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system

    Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.

    FDA · DeviceCareFusion 303, Inc.Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
  7. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H938176, for use in a pharmaceutical compounding device

    Baxter Healthcare Corporation has received increased customer reports of particulate matter in the Automated Compounding Device Inlets (disposable inlet), Product Codes H938173, H938174, H938175, H938176, used with the…

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution.Official notice →
See all drugs & medical recalls →