Drugs & medicalClass II

Maquet Cardiopulmonary Gmbh recalls Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.

Device does not comply with the labeling requirements of international standard IEC 60601-1.

Read the official notice →
Date
2025-08-06
Country
United States
Brand
Maquet Cardiopulmonary
Product
Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.
Classification
Class II
Units
Worldwide distribution - US Nationwide and the countries of Australia, New…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Maquet Cardiopulmonary recalls

  1. 2026-09-23
  2. US
    Drugs & medicalClass II

    Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS);

    The packaging may not consistently maintain sterile barrier integrity.

    FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →
  3. 2026-02-11
  4. US
    Drugs & medicalClass II

    Maquet Cardiopulmonary Gmbh recalls Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;

    Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending of the connecting cable can lead to full damage of the…

    FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide Distribution: US (Nationwide) and OUS (International) to countries…Official notice →
  5. 2025-06-04
  6. US
    Drugs & medicalClass II

    Maquet Cardiopulmonary Ag recalls Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital transport by…

    HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.

    FDA · DeviceMaquet Cardiopulmonary AgDomestic: IL & MO. Foreign: Australia, Austria, Belgium, Canada, China,…Official notice →
All 4 Maquet Cardiopulmonary recalls →

Other drugs & medical recalls in the United States

  1. 2025-08-06
  2. US
    Drugs & medicalClass II

    Capnia Inc recalls Precision Sampling Set, REF: C20206 for use with the CoSense End-Tidal Carbon Monoxide Monitor

    Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO) monitor may have residual carbon monoxide and volatile organic compounds present due to insufficient aeration of the cannula's carbon filter prior…

    FDA · DeviceCapnia IncUS Nationwide distribution in the states of PA, UT, TX, FL, MA, IA.Official notice →
  3. US
    Drugs & medicalClass II

    LTS Therapy Systems, LLC recalls IontoPatch 80, On-the-Go Patch Therapy, Model/Catalog Number: D-0077-080; The IontoPatch is an Iontophoresis transdermal patch.

    The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device.

    FDA · DeviceLTS Therapy Systems, LLCUS Nationwide distribution in the states of Indiana, Tennessee, New York,…Official notice →
  4. US
    Drugs & medicalClass II

    Microbiologics Inc recalls LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894K (6-pack), 2) REF 0894P (2-pack)

    KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.

    FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide and the countries of France, Colombia,…Official notice →
  5. US
    Drugs & medicalClass II

    Phasor Health, LLC recalls Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35

    Drill for use in neurosurgical procedures may have a reverse battery orientation, which may increase surgical time.

    FDA · DevicePhasor Health, LLCUS: PA, IN, AZ, MO, LA, FL, TX, MA, OH, TN, MI, WV, VA, CA, DE, NH, GA, SC,…Official notice →
  6. US
    Drugs & medicalClass II

    Boston Foundation For Sight recalls BostonSight SCLERAL Lens

    Select orders of lenses were manufactured with errors impacting sagittal height, haptics, or both.

    FDA · DeviceBoston Foundation For SightWorldwide distribution - US Nationwide and the countries of Canada.Official notice →
  7. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10, Model Number: 722026. 2. Allura Xper…

    Potential for temporary loss of imaging (X-ray) functionality due to software issue.

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide - US Nationwide and the countries of Algeria, Argentina, Australia,…Official notice →
See all drugs & medical recalls →