Drugs & medicalClass II

MEDLINE INDUSTRIES, LP - Northfield recalls Medline Leg bag, REF URO12573

Undeclared latex

Read the official notice →
Date
2023-12-20
Country
United States
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product
Medline Leg bag, REF URO12573
Classification
Class II
Units
US and Panama
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2024-02-07
  2. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723

    Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution.Official notice →
  3. 2024-01-17
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline Gown Poly W/Breath Sleeves XL AAMIK Level 4 (Eclipse gown), REF SPT-2208CS, 100/pack, Non-Sterile.

    Surgical gowns were manufactured with the wrong sleeve.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldDistribution was made to MD, OH, TN, TX, and WI. There was no…Official notice →
  5. 2024-01-03
  6. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray with 14 Fr Suction Catheter, REF DYND40580, Sterile;…

    The component tracheostomy brush has a sharp edge at the tip that can potentially puncture tubing during use and/or cause user injury. Additionally, there have been incidents of the tracheostomy brush bristles…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution including Puerto Rico. OUS (Foreign) distribution…Official notice →
  7. 2023-12-20
  8. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls STERILE PVP SOLUTION, REF DYNDA1907

    The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.Official notice →
  9. 2023-11-22
  10. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245

    This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of California.Official notice →
  11. 2023-11-15
  12. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Clinical TREAT Antifungal Powder, Vanilla Scent, 3 OZ (85 g) tube, Active Ingredient: Miconazole Nitrate 2.0% w/w…

    CGMP deviations: the product was shipped from the Manufacturer to a Medline warehouse and released to stock while it was still under investigation for low assay results on the active ingredient miconazole nitrate.

    FDA · DrugMEDLINE INDUSTRIES, LP - NorthfieldNationwideOfficial notice →
All 117 MEDLINE INDUSTRIES, LP - Northfield recalls →

Other drugs & medical recalls in the United States

  1. 2023-12-20
  2. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls Baxter Amia Automated Peritoneal Dialysis (APD) Cycler Set, REF 5C5479

    There is to an increase in complaints related to failure alarms for Wet Cassette Integrity Test occurring on the Amia devices.

    FDA · DeviceBaxter Healthcare CorporationWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  3. US
    Drugs & medicalClass I

    Integra LifeSciences Corp. recalls CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP) Monitor, Model…

    Firm is expanding the existing recall RES 90457 for the Cerelink, initiated in June 2022, to include all CereLink ICP Extension Cables. The updated corrective action includes a design change to the extension cable to…

    FDA · DeviceIntegra LifeSciences Corp.US distribution nationwide to the following states: AL AR AZ CA CO CT DC DE FL…Official notice →
  4. US
    Drugs & medicalClass II

    Ortho-Clinical Diagnostics, Inc. recalls VITROS XT 3400 Chemistry System Product Code 6844458 Running Software Version 3.8.0

    During planned monitoring of data post-release of Software Version 3.8.0 an increased occurrence of software issues relating to unresponsive subsystems, unresponsive user interface (sometimes referred to as a screen…

    FDA · DeviceOrtho-Clinical Diagnostics, Inc.US Nationwide. Global Distribution.Official notice →
  5. US
    Drugs & medicalClass II

    Encore Medical, LP recalls RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

    Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver

    FDA · DeviceEncore Medical, LPU.S.: AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, Puerto Rico, RI, SC, TN, TX,…Official notice →
  6. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls STERILE PVP SOLUTION, REF DYNDA1907

    The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of CT, IA, LA, MA, PA, CA, NY, FL.Official notice →
  7. US
    Drugs & medicalClass II

    Limacorporate S.p.A recalls PHYSICA HPS Tibial Liner #6 H10 REF 6539.54.610

    Due to incorrect product labeling

    FDA · DeviceLimacorporate S.p.AU.S Distribution: AZ, CA, IL, LA, and NYOfficial notice →
See all drugs & medical recalls →