Reported Mar 18, 2020 · Terminated
Monoject Bluntfill with Filter, 18G x 1-1/2" Item Code 11811022F. Used for drawing fluid from a vial - Product Usage:…
Cardinal Health 200, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Cardinal Health 200, LLC · 15 Hampshire St Bldg 5 · Mansfield, MA · 02048-1113
Is this the product you have?
- Monoject Bluntfill with Filter, 18G x 1-1/2" Item Code 11811022F. Used for drawing
- fluid from a vial - Product Usageused for general purpose injection and aspiration of fluids from vials, ampules and parts of the body below the surface of the skin
- Lot codes and dates
Lot No. 15072024Item Code 11811022FExpires 06/20/2020
- Amount recalled
- 8000
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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