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Recall Observatory FDA recall evidence

Drug product

FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution), Net 1.1 mL and 1 SEPP (povidone iodine 10% USP), Net 0.67 mL per kit, packaged in 20 kits per carton, Cat. No 260288, NDC 54365-202-99, CareFusion, Leawood, KS 66211.

D-229-2013

March 04, 2013

Class II

Product summary

Firm
CareFusion 213, LLC
Event
Event 64583
Status
Terminated
Classification
Class II
Quantity
544,500 kits
Official record key
drug-enforcement:D-229-2013

Official wording

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.

Code information: All lots with expiry between 07/11 to 08/14.

Distribution pattern: Nationwide, Puerto Rico, Virgin Islands, Malaysia, and United Kingdom

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    misbranded