Drugs & medicalClass II

MEDLINE INDUSTRIES, LP - Northfield recalls meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus…

The product was incorrectly shipped at room temperature rather than refrigerated.

Read the official notice →
Date
2022-03-02
Country
United States
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product
meridian bioscience immunocard STAT! Rotavirus test, REF 750030, 30 tests/kit box. The ImmunoCard STAT! Rotavirus Immunoassay is a rapid…
Classification
Class II
Units
US Distribution was made to IL, FL, LA, MS, NC, OH, and TX.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2022-04-20
  2. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)

    Product was improperly store which may cause a delay in results.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS distribution only - AL, CA, FL, GA, IL, IN, LA, MO, MS, NC, NE, NY, OH, PA,…Official notice →
  3. 2022-04-13
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Excelsior Medical 10mL Sterile Field Saline Flush ZR, 0.9% Sodium Chloride Injection, USP, REF EMZ10091280, Sterile, IV…

    Sterility failure of the exterior of the syringe which may impact the device's ability to be laid on a sterile field.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide Distribution was made to KY, OK, and TX. There was no…Official notice →
  5. 2022-03-09
  6. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes

    Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Panama and Bermuda.Official notice →
  7. 2022-03-02
  8. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Michels Transport Medium, 20ML Prefilled Cont

    Product stored incorrectly in temperature controlled setting instead of refrigeration.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of Colorado, Florida, New York, North…Official notice →
  9. 2022-02-16
  10. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls CURAD REUSABLE GEL HOT/COLD PACK

    The product contains natural rubber latex but the label states that it does not.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS and Bahamas, Bermuda, Panama, Lebanon, Barbados, Honduras, AnguillaOfficial notice →
  11. 2022-02-09
  12. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls HARDY DIAGNOSTICS CatScreen, 25dsk/vial

    Product stored incorrectly in temperature controlled setting instead of refrigeration.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of California.Official notice →
All 117 MEDLINE INDUSTRIES, LP - Northfield recalls →

Other drugs & medical recalls in the United States

  1. 2022-03-09
  2. US
  3. US
  4. US
  5. 2022-03-02
  6. US
    Drugs & medicalClass II

    Biomet, Inc. recalls Comprehensive Shoulder System Primary Shoulder Stem, Micro Length, Porous Plasma, 11 MM, 55 MM Long Item Number: 113611

    The products in scope underwent an incorrect rework operation for the porous plasma sprayed coating. Internal testing indicated that the parts may not have sufficient adhesion strength. The scope was identified to be…

    FDA · DeviceBiomet, Inc.Worldwide distribution - US Nationwide and the countries of Canada, Ecuador,…Official notice →
  7. US
    Drugs & medicalClass II

    Collagen Matrix, Inc. recalls DuraMatrix-Onlay Collagen Dura Substitute Membrane 4 inches x 5 inches (10.0cm x 12.5cm) REF: CDSLM45

    Outer packaging (outer pouch) is not sealed compromising sterility and result in potential risk of patient infection, which could lead to revision surgery

    FDA · DeviceCollagen Matrix, Inc.DuraMatrix-Onlay distributed US Nationwide in the states of FL, IN, Puerto…Official notice →
  8. US
    Drugs & medicalClass II

    C.R. Bard Inc recalls BARD SURESTEP INTERMITTENT CATHETER TRAY, 14Fr, REF INTS14C

    There is a potential to leak from the catheter where it connects to the drain bag

    FDA · DeviceC.R. Bard IncUS Nationwide distribution in the states of GA, ME, NJ, WI, MN, SD, CO, ND,…Official notice →
See all drugs & medical recalls →