🔍 RecallPedia

Medline CC Drawer 4 IV Circulation Pack, Contains Rx, Single Use Only, contains 2 Prep Pad PVPs. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

Class I - Dangerous
💊 Drugs Recalled: September 21, 2017 Medline Industries Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Pack Number: ACC010254A; Lots: 17HD4376; 17HD1709; 17HD1709
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Medline Industries Inc
Reason for Recall:
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Medline CC Drawer 4 IV Circulation Pack, Contains Rx, Single Use Only, contains 2 Prep Pad PVPs. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093

Product Codes/Lot Numbers:

Pack Number: ACC010254A; Lots: 17HD4376; 17HD1709; 17HD1709

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0253-2018

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