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Class II: temporary or reversible health riskTerminated

CareFusion 213 Blood Culture Prep Kit II containing 1 FREPP Recall

Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol)

CareFusion 213, LLC · El Paso, TX

Risk level
Class II
Reported by FDA
Apr 3, 2013
Recall ID
D-227-2013
Check your lot numberHow we source this data

Summary

CareFusion 213 recalled Blood Culture Prep Kit II containing 1 FREPP starting Mar 4, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-227-2013 on Apr 3, 2013. Reason: Labeling: Not Elsewhere Classified: This product is misbranded because the product is not sterile and the labeling is misleading in relation to sterility claims. Status: Terminated.

Why it was recalled

Labeling: Not Elsewhere Classified: This product is misbranded because the product is not sterile and the labeling is misleading in relation to sterility claims.

Product description

Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol), Net 1.1 mL and 1 SEPP (iodine tincture 2% USP), Net 0.67 mL per kit, packaged in 20-count kits per carton, Cat. No 260307, NDC 54365-200-99, CareFusion, Leawood, KS 66211.

Lot numbers, UPCs & expiration codes

All lots with expiry between 12/11 to 10/15.

Where it was sold

Nationwide, Puerto Rico, Virgin Islands, Malaysia, and United Kingdom

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-227-2013
Classification
Class II
Status
Terminated
Recall initiated
Mar 4, 2013
FDA report date
Apr 3, 2013
Quantity
929,000 kits
Recall type
Voluntary: Firm initiated
Recalling firm
CareFusion 213, LLC

Original FDA data

Every field from FDA enforcement report D-227-2013, exactly as published.

Show all FDA fields
City
El Paso
State
TX
Status
Terminated
Country
United States
Event ID
64583
Address
1550 Northwestern Drive
Code information
All lots with expiry between 12/11 to 10/15.
Postal code
79912-8000
Report date
Apr 3, 2013
Product type
Drugs
Recall number
D-227-2013
Classification
Class II
Recalling firm
CareFusion 213, LLC
Product quantity
929,000 kits
Termination date
May 12, 2014
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Blood Culture Prep Kit II containing 1 FREPP (70% isopropyl alcohol), Net 1.1 mL and 1 SEPP (iodine tincture 2% USP), Net 0.67 mL per kit, packaged in 20-count kits per carton, Cat. No 260307, NDC 54365-200-99, CareFusion, Leawood, KS 66211.
Distribution pattern
Nationwide, Puerto Rico, Virgin Islands, Malaysia, and United Kingdom
Recall initiation date
Mar 4, 2013
Initial firm notification
Letter
Center classification date
Mar 28, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-227-2013, published Apr 3, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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