Drugs & medicalClass II

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.

Read the official notice →
Date
2024-12-04
Country
United States
Brand
Baxter Healthcare
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Classification
Class II
Units
Worldwide 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 Details may be shortened or out of date; the official notice is the authoritative source.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 Baxter Healthcare recalls

  1. 2025-01-29
  2. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519

    Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of MN, MO, VA, TX, CA, MA, FL, SC.Official notice →
  3. 2025-01-22
  4. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002

    There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

    FDA · DeviceBaxter Healthcare CorporationUS, Nationwide DistributionOfficial notice →
  5. 2025-01-08
  6. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2

    Devices were identified as released after repair without full testing being performed, which includes flow testing.

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of AL, IN.Official notice →
  7. 2024-11-27
  8. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

    Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using…

    FDA · DeviceBaxter Healthcare CorporationWorldwide Distribution (US Nationwide distribution)Official notice →
  9. 2024-11-20
  10. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

    The door on the Spectrum IQ Infusion pump may not be able to fully close.

    FDA · DeviceBaxter Healthcare CorporationGA, IDOfficial notice →
  11. US
    Drugs & medicalClass I

    Baxter Healthcare Corporation recalls Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is Vantive.

    Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using…

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution and worldwideOfficial notice →
All 123 Baxter Healthcare recalls →

Other drugs & medical recalls in the United States

  1. 2024-12-04
  2. US
    Drugs & medicalClass II

    Gauthier Biomedical, Inc. recalls TriALTIS TORQUE LIMITER, RATCHET, 11.3 Nm, Model Number 5161-00-5048 (G919509)

    An out of specification component may result in the device exhibiting torque output higher than the design specification.

    FDA · DeviceGauthier Biomedical, Inc.US Nationwide distribution in the state of MA.Official notice →
  3. US
    Drugs & medicalClass II

    LivaNova Deutschland GmbH recalls Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software

    Heart-Lung Machine GUI touchscreen may go dark for 10-15 seconds, safety/performance functions remain operational before reset, control maintained through backup control panel, but second reset may occur, may lead to…

    FDA · DeviceLivaNova Deutschland GmbHUS Nationwide distribution in the states of CA, VA, GA, IN, NJ, FL, CO, MS, NV.Official notice →
  4. US
    Drugs & medicalClass II

    Securitas Healthcare LLC recalls Arial Server Software Versions 11.1.4 through 11.1.6, SKU 54305, in conjunction with the Arial Mobile Application or Arial Care Giver…

    Certain software versions will not notify end users of calls initiated by call points with the Arial Emergency and Nurse Call System.

    FDA · DeviceSecuritas Healthcare LLCWorldwide distribution - US Nationwide and the countries of Canada, Switzerland.Official notice →
  5. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls ENDO KIT, Medline Kit SKU DYKE1577A, Component Number 57469, 10 per case; Medline Convenience Kits containing Single Use…

    Identified lots of Olympus product may be missing sterile and manufacturing lot numbers and expiration dates on the sterile packaging. The information can be found on the outer box or zipper bag label. Medline is…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of NY.Official notice →
  6. US
    Drugs & medicalClass III

    Remote Diagnostic Technologies Ltd. recalls Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual or…

    Due to incorrect labels applied to devices during servicing. Labels contain the incorrect product name and CAT number.

    FDA · DeviceRemote Diagnostic Technologies Ltd.U.S. Nationwide distribution in the states of AL, CA, FL, MO, NY, OH, TX and VA.Official notice →
  7. US
    Drugs & medicalClass II

    Shimadzu Corp. Analytical & Measuring Instruments Div. recalls Autosampler, Models: SIL-40C XR CL, SIL-40C X3 CL

    There have been cases of failure of the main board due to condensation water occurring in the gap between thermal insulation material on the underside of the main base dropping onto the main board The symptoms and…

    FDA · DeviceShimadzu Corp. Analytical & Measuring Instruments Div.Worldwide - US Nationwide distribution in the states of DE, PA and the country…Official notice →
See all drugs & medical recalls →