FDAJanuary 15, 2020device

Monoject Bluntfill with Filter, 18G x 1-1/2" Item Code 11811022F. Used for drawing fluid from a vial - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Non-sterile product was shipped to customers. Product package is labeled as both "STERILE" and "NON-STERILR" ; the product did not undergo sterilization process and is non-sterile. The usage of a needle that is not sterile could result in infection. Firm is not aware of any reports of patient harm.

What to do

FDA enforcement status: Terminated

Brands named

cardinal health 200cardinalcardinal health

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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