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.

Read the official notice →
Date
2025-03-26
Country
United States
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product
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 DRAPE,12/CS;…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 MEDLINE INDUSTRIES, LP - Northfield recalls

  1. 2025-04-02
  2. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) C SCOPE DISPOSABLE KIT, Pack Number 613034700, 2) C SCOPE DISPOSABLE KIT, Pack Number…

    Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  3. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls namic convenience kits labeled as: 1) MTS,4 VALVE,LFT,HRT,KIT-AHS-A*,NW, REF 60010468; 2) MTS,RIGHT HEART,KIT,W/TRANS,ST. *,…

    The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of The Netherlands,…Official notice →
  4. 2025-03-26
  5. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits labeled as: 1) EYE PACK, Pack Number VAL038BSCLC

    Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide - US Nationwide and the country of Canada.Official notice →
  6. US
  7. 2025-02-26
  8. 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 →
  9. US
    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…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS: CAOfficial notice →
All 117 MEDLINE INDUSTRIES, LP - Northfield recalls →

Other drugs & medical recalls in the United States

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

    CareFusion 303, Inc. recalls BD Pyxis: Anesthesia Station ES, REF: 327, MedStation ES, REF: 323, MedStation ES Tower, REF: 352, CII Safe ES, REF: 1116-00, CII Safe ES…

    Sync timeout may occur between the server and automated dispensing device, due to a server software error which may occur if syncing a large amount of data that takes excessive time, which may cause the dispensing…

    FDA · DeviceCareFusion 303, Inc.Worldwide - US Nationwide distribution including in the states of KY, OH, NY,…Official notice →
  3. US
    Drugs & medicalClass II

    Waldemar Link GmbH & Co. KG (Mfg Site) recalls Modular Stem cylindrical, Tilastan¿, press-fit cementless, L= 80 mm, DIA = 11 mm, Product Code: 880-601/11

    A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.

    FDA · DeviceWaldemar Link GmbH & Co. KG (Mfg Site)Worldwide - US Nationwide distribution in the states of AL, CA, CO, FL, GA,…Official notice →
  4. US
    Drugs & medicalClass II

    Microbiologics Inc recalls Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus (Pellet), Multi-analyte, unassayed quality control material, Catalog…

    The A549 human cell target (human cells for sample adequacy control) may give a late Ct value.

    FDA · DeviceMicrobiologics IncUS Nationwide distribution in the states of TX. UK.Official notice →
  5. US
    Drugs & medicalClass II

    American Contract Systems Inc recalls MAJOR VASCULAR PACK , Model No UTMV78X-01 UTMV78Y UTMV78Y-01 UTMV78X-01 UTMV78Y-02

    ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

    FDA · DeviceAmerican Contract Systems IncUS Nationwide distribution in the state of OH.Official notice →
  6. US
    Drugs & medicalClass I

    Smiths Medical ASD, Inc. recalls smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems, 82-24

    The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.

    FDA · DeviceSmiths Medical ASD, Inc.Worldwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Mylan Institutional, Inc. recalls Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg), Rx Only, 100 Unit Dose Blister Cards of 10 (10 cards of 10 tablets each) per…

    Super-Potent Drug: Out of specification potency results were obtained.

    FDA · DrugMylan Institutional, Inc.Nationwide in the USAOfficial notice →
See all drugs & medical recalls →