Drugs & medicalClass II

MEDLINE INDUSTRIES, LP - Northfield recalls Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397; medical procedure convenience kit

Medline is recalling medical convenience kits which were assembled with specific Coloplast Foley catheters and Prostatic catheters which were subsequently recalled due to a potential sterility issue detected during…

Read the official notice →
Date
2025-02-26
Country
United States
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product
Medline RR-LIVER TRNS ACCESSORY PEDS, DUNJ63397; medical procedure convenience kit
Classification
Class II
Units
US: CA
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 Details may be shortened or out of date; the official notice is the authoritative source.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 MEDLINE INDUSTRIES, LP - Northfield recalls

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

    MEDLINE INDUSTRIES, LP - Northfield recalls Proxima Drape labeled as PACK,BASIC,SIRUS,V,5/CS; PACK,BASIC IV,SIRUS,5/CS; PACK,SET UP,NO DRAPE,12/CS; PACK,SET UP,NO…

    Potential breach in pouch packaging which could lead to loss of sterility.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution.Official notice →
  3. US
  4. 2025-02-26
  5. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP.…

    Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS States: CA, NYOfficial notice →
  6. 2025-02-05
  7. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ARTERIAL LINE PACK, REF DYNJ65208B, medical convenience kit containing Infusion Catheter with Antimicrobial Heparin…

    Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS: FL, KS, ND, PA, WA, WV, IL, WAOfficial notice →
  8. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) CENTRAL LINE DRESSING KIT, Reorder number DYNDC3189; dressing change tray

    Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the bioburden testing requirements of…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution.Official notice →
  9. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690

    The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide.Official notice →
All 117 MEDLINE INDUSTRIES, LP - Northfield recalls →

Other drugs & medical recalls in the United States

  1. 2025-02-26
  2. US
    Drugs & medicalClass II

    XTANT Medical Holdings, Inc recalls Irix-A Integrated Lumbar Fusion System, Model Number X080-423011-08PC (Spacer Assy, 42 X 30 X 8¿, 11mm, PC (STERILE)) and Model…

    Certain implants in the Irix-A Lumbar Fusion System were distributed while labeled with an incorrect expiration date.

    FDA · DeviceXTANT Medical Holdings, IncWorldwide - US Nationwide distribution in the states of AZ, CA, CO, LA, OH,…Official notice →
  3. US
    Drugs & medicalClass II

    KCI USA, INC. recalls 3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit VIAKIT07S05/AU - V.A.C. VIA Starter Kit…

    Due to increase in complaints related to leak alarms

    FDA · DeviceKCI USA, INC.Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
  4. US
    Drugs & medicalClass II

    DeRoyal Industries Inc recalls DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement

    The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.

    FDA · DeviceDeRoyal Industries IncU.S.: ND, NY, VA, WV, NJ, TN, OK, TN, GA, OH, MN, AZ, WI, IL, MA, MD, MO, AR,…Official notice →
  5. US
    Drugs & medicalClass II

    Augustine Temperature Management, LLC recalls Augustine Surgical Inc. HotDog Return Electrode accessory connector cables, Model A138 used in conjunction with Warming…

    Users were experiencing the following error message (M-0B-125) stated Check Neutral Electrode Contact .

    FDA · DeviceAugustine Temperature Management, LLCUS distribution to states of: AL, TX, NVOfficial notice →
  6. US
    Drugs & medicalClass I

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013.

    Possibility of the patient falling from the table related to the mattress used on the patient table.

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldiwde distribution - US Nationwide and the countries of Afghanistan,…Official notice →
  7. US
    Drugs & medicalClass I

    Spectranetics Corporation recalls Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,1.5-4.5mm),…

    Use of Tack Endovascular system, designed to treat acute dissections of inner wall or lining of an artery by tacking damaged tissue to inner luminal surface, could result in problems with deployment and stability of…

    FDA · DeviceSpectranetics CorporationDistribution US nationwide and countries of: NL, DE, NL, AU, IT, CH, GB, and ATOfficial notice →
See all drugs & medical recalls →