Drugs & medicalClass II

Medline Industries, LP recalls Medline medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: 1. BLOOD CULTURE KIT, Medline Kit SKU DYNDH1520;…

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be…

Read the official notice →
Date
2026-05-06
Country
United States
Brand
Medline Industries
Product
Medline medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: 1. BLOOD CULTURE KIT, Medline Kit SKU DYNDH1520;…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 recalls

  1. 2026-06-03
  2. US
    Drugs & medicalClass I

    Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2)…

    Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and…

    FDA · DeviceMedline Industries, LPWorldwide - US Nationwide distribution in the US Territory of Virgin Islands…Official notice →
  3. 2026-05-20
  4. US
    Drugs & medicalClass I

    Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B

    Medline has identified the presence of particulate within the fluid path of the Manifolds.

    FDA · DeviceMedline Industries, LPUS (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.Official notice →
  5. 2026-05-13
  6. US
    Drugs & medicalClass II

    Medline Industries, LP recalls See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) BREAST-HERNIA-PORT CDS-LF,…

    Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified…

    FDA · DeviceMedline Industries, LPWorldwide - US Nationwide distribution.Official notice →
  7. 2026-05-06
  8. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.25" X 0.25", XR, 10/PK,…

    During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

    FDA · DeviceMedline Industries, LPWorldwide distribution.Official notice →
  9. 2026-04-29
  10. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ909398A ROBOTIC PACK…

    Unapproved design changes to the products outside of the 510(k) clearance.

    FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the countries of Canada, Panama,…Official notice →
  11. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model Number: DYNJ37543A

    The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution.Official notice →
All 75 Medline Industries recalls →

Other drugs & medical recalls in the United States

  1. 2026-05-13
  2. US
    Drugs & medicalClass II

    Ajanta Pharma Ltd. recalls Duloxetine Delayed-Release Capsules, 30 mg, Rx Only, a) 90 Capsules, NDC 27241-098-09, b) 30 capsules, NDC 27241-098-03, c) 1000 Capsules,…

    CGMP Deviations: Presence of N-nitroso-Duloxetine impurity above FDA recommended limit of 0.83 ppm, identified at the 12-month and 18-month long-term stability intervals.

    FDA · DrugAjanta Pharma Ltd.Nationwide within U.SOfficial notice →
  3. US
    Drugs & medicalClass II

    Fresenius Medical Care Holdings, Inc. recalls DELFLEX, Dextrose Peritoneal Dialysis Solution with attached stay-safe Exchange Set for Intraperitoneal Dialysis Only,…

    Lack of Assurance of Sterility: Potential leaks from perforations in bags.

    FDA · DrugFresenius Medical Care Holdings, Inc.Nationwide in the USAOfficial notice →
  4. US
  5. 2026-05-06
  6. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.25" X 0.25", XR, 10/PK,…

    During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.

    FDA · DeviceMedline Industries, LPWorldwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Elekta, Inc. recalls Brand Name: Leksell Vantage Arc System REF: 1053958

    Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.

    FDA · DeviceElekta, Inc.US: AR AZ CA CO DC FL GA ID IL KS MA MD ME MO MT NC NE NH NJ NM NV NY OH OK PA…Official notice →
  8. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics Inc recalls epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;

    Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial, venous, and capillary patient samples. An erroneously low…

    FDA · DeviceSiemens Healthcare Diagnostics IncWorldwide distribution - US Nationwide and the countries of Italy, Spain,…Official notice →
See all drugs & medical recalls →