SEPP 10% Povidone Iodine Solution USP (1% available Iodine, Surfactant & USP Purified Water), packaged in a) 200-count applicators (Net 0.67 mL each) per carton, CareFusion, Leawood, KS 66211, Cat. No 260286, NDC 54365-145-01; and b) 3000-count applicators per case, Cat. No 260681, CareFusion, Leawood, KS 66211.

Class I - Dangerous
💊 Drugs Recalled: March 4, 2013 CareFusion 213 Other Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    a) All lots with expiry between 09/12 to 10/15 and b) All lots with expiry between 10/11 to 07/14.
  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:
CareFusion 213, LLC
Reason for Recall:
Labeling: Not Elsewhere Classified: This product is misbranded because the product is not sterile and the labeling is misleading in relation to sterility claims.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

SEPP 10% Povidone Iodine Solution USP (1% available Iodine, Surfactant & USP Purified Water), packaged in a) 200-count applicators (Net 0.67 mL each) per carton, CareFusion, Leawood, KS 66211, Cat. No 260286, NDC 54365-145-01; and b) 3000-count applicators per case, Cat. No 260681, CareFusion, Leawood, KS 66211.

Product Codes/Lot Numbers:

a) All lots with expiry between 09/12 to 10/15 and b) All lots with expiry between 10/11 to 07/14.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-226-2013

Related Recalls

Lack of Assurance of Sterility: The affected product may exhibit an open seal on the packaging of the applicator.

May 15, 2025 Compounded Drugs Nationwide View Details →

Non-Sterility: contamination of Aspergillus penicillioides, due to breach in package lidding.

Feb 14, 2025 Compounded Drugs Nationwide View Details →

Stability data does not support expiry: Shelf-life of the impacted lots of BD ChloraPrep" Clear 1 mL Applicator cannot be substantiated beyond 12-months although labeled with 36-month expiry. Stability studies indicate that the impacted lots, if stored at 30¿C/75% relative humidity continuously beyond 12 months, may exhibit growth of Aspergillus penicillioides.

Aug 25, 2023 Compounded Drugs Nationwide View Details →