Drugs & medicalClass II

MEDLINE INDUSTRIES, LP - Northfield recalls Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395

Three is the potential for the retractors to puncture through the sterile packaging.

Read the official notice →
Date
2025-05-21
Country
United States
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2025-07-09
  2. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV…

    Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the Catheter, the needle is slow…

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the states of IN, KY, CA, MI, TX, WA.Official notice →
  3. 2025-07-02
  4. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250

    There is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of VA.Official notice →
  5. 2025-06-11
  6. US
    Drugs & medicalClass I

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU…

    Affected kits contain recalled Integra Lifesciences Codman Disposable Perforators due to inadequate welds on specific lots. Perforators with inadequate welds may break or separate.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS distribution to CA, FL, IL, IN, KY, MA, MD, MN, NY, TX, VT, WA and WI. No…Official notice →
  7. 2025-05-14
  8. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits, Model Number 750830

    A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was inadvertently stored in Medline warehouses at temperatures outside of the labeled storage requirements.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution.Official notice →
  9. 2025-05-07
  10. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: T AND A PACK -LF, REF DYNJ85792

    It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Panama and Canada.Official notice →
  11. 2025-04-23
  12. US
    Drugs & medicalClass II

    MEDLINE INDUSTRIES, LP - Northfield recalls Medline Convenience kits used for various procedures: 1) NAIL PACK, Model Number: SUT15830A;

    There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

    FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldWorldwide distribution - US Nationwide and the countries of Canada, Mexico,…Official notice →
All 117 MEDLINE INDUSTRIES, LP - Northfield recalls →

Other drugs & medical recalls in the United States

  1. 2025-05-21
  2. US
    Drugs & medicalClass II

    Beckman Coulter Inc. recalls DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065. The Beckman Coulter…

    Beckman Coulter is recalling their DxC 500 AU Clinical Chemistry Analyzer because a software error causes the analyzer to not run a requested calibration order in the following scenario: when a reagent blank or…

    FDA · DeviceBeckman Coulter Inc.U.S: AL, CA, GA, ID, IN, LA, MA, MI, MN, MT, NC, NV, PA, PR, TN , TX, and WI…Official notice →
  3. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Intera 1.5T Master/Nova, Model Number: 781106;

    The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin…

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.US: Nationwide Distribution International: Algeria, Andorra, Argentina,…Official notice →
  4. US
    Drugs & medicalClass II

    Klinika Mdical Gmb recalls KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device…

    Potential for microbial contamination.

    FDA · DeviceKlinika Mdical GmbUS Nationwide distribution in the state of Massachusetts.Official notice →
  5. US
    Drugs & medicalClass II

    Contec Medical Systems Co., Ltd. recalls CMS8000 Patient Monitor

    Patient monitor has nine identified cybersecurity vulnerabilities.

    FDA · DeviceContec Medical Systems Co., Ltd.US Nationwide distribution in the states of CA, IL, FL, KY, TX.Official notice →
  6. US
    Drugs & medicalClass II

    ICU Medical, Inc. recalls LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2

    Firm has identified Drug Library Management defects in the software: 1) DLM software does not allow user to create percentage dose rate or rate change values with certain limits, potentially resulting in over-delivery…

    FDA · DeviceICU Medical, Inc.Worldwide - US Nationwide distribution in the states of CA, FL, IA, KY, LA,…Official notice →
  7. US
    Drugs & medicalClass II

    Cook Incorporated recalls Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular…

    Cook Medical identified that devices from the affected device lots may contain the incorrectly sized embolization coil.

    FDA · DeviceCook Incorporatedworldwide - No US distribution.Official notice →
See all drugs & medical recalls →