Drugs & medicalClass I

Cardinal Health 200, LLC recalls Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.

Non-Sterility: microbial contamination identified as Paenibacillus phoenicis

Read the official notice →
Date
2026-03-25
Country
United States
Brand
Cardinal Health
Product
Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes, Cardinal Health 200 LLC 3651 Birchwood Drive, Waukegan, IL 60085.
Classification
Class I
Units
Nationwide within the United States, Puerto Rico and Japan.
Category
Drugs & medical
Source
FDA · Drug

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 Details may be shortened or out of date; the official notice is the authoritative source.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 Cardinal Health recalls

  1. 2026-09-09
  2. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) PBCGLVBLI, Catalog Number: KIT, BLO LAVH ; 2)…

    The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin…

    FDA · DeviceCardinal Health 200, LLCUS Nationwide distribution.Official notice →
  3. 2026-08-19
  4. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Cardinal Health Presource Kits: 1) ENT TRAY , Catalog Number: 24-0726A; 2) KIT,SINUS , Catalog Number: PE13SPAJA; 3) KIT,SINUS , Catalog…

    Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.

    FDA · DeviceCardinal Health 200, LLCUS Nationwide. Canada.Official notice →
  5. 2026-04-08
  6. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777

    The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are U-100 Insulin syringes.

    FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  7. 2026-02-04
  8. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health Sentinel Seal CDU 2. 8888571513 Cardinal…

    The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older. When used on infants, the CDU may not demonstrate…

    FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide and the countries of Brazil, Canada,…Official notice →
  9. 2025-12-17
  10. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-sterile; CT5502T…

    Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the product packaging as five (5) years.

    FDA · DeviceCardinal Health 200, LLCWorldwide distribution - US Nationwide and the country of Canada.Official notice →
  11. 2025-10-29
  12. US
    Drugs & medicalClass II

    Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3…

    Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

    FDA · DeviceCardinal Health 200, LLCWorldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →
All 41 Cardinal Health recalls →

Other drugs & medical recalls in the United States

  1. 2026-03-25
  2. US
    Drugs & medicalClass II

    Howmedica Osteonics Corp. recalls MICS3 Angled Sagittal Saw Attachment; Part Number: 210490

    A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and…

    FDA · DeviceHowmedica Osteonics Corp.Domestic: Nationwide Distribution; International: Australia, Germany, Belgium,…Official notice →
  3. US
    Drugs & medicalClass II

    GE Medical Systems, LLC recalls Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and…

    There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized…

    FDA · DeviceGE Medical Systems, LLCWorldwide - US Nationwide distribution.Official notice →
  4. US
    Drugs & medicalClass II

    Abbott Diagnostics Scarborough, Inc. recalls Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description:…

    It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.

    FDA · DeviceAbbott Diagnostics Scarborough, Inc.US Nationwide distribution.Official notice →
  5. US
  6. US
    Drugs & medicalClass II

    SOMERSET THERAPEUTICS LLC recalls Dexamethasone Sodium Phosphate Injection, USP, 100 mg/ 10 mL, (10 mg/mL), 10x10 mL Multiple Dose Vials, Rx only, Manufactured for:…

    Failed Impurities/Degradation Specifications - OOS impurities result observed during long term stability testing at product expiry (24 months) were above specs for these impurities: Dexamethasone Sodium Phosphate EP…

    FDA · DrugSOMERSET THERAPEUTICS LLCNationwide in the USAOfficial notice →
  7. US
    Drugs & medicalClass III

    Annora Pharma Private Limited recalls Pitavastatin Tablets, 2 mg, packaged in 90-count bottles, Rx only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141,…

    Presence of foreign tablets/capsules: one Pitavastatin tablet 1mg found in bottle of Pitavastatin tablets 2mg

    FDA · DrugAnnora Pharma Private LimitedTNOfficial notice →
See all drugs & medical recalls →