Reported Nov 6, 2019 · Terminated
DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03
Valeritas, Incorporated
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: Valeritas, Incorporated · 293 Boston Post Rd W Ste 330 · Marlborough, MA · 01752-4615
Is this the product you have?
DEMO No Needle Corrugated Carton 20 U/DPart Number 2260-03
- Lot codes and dates
- UDI(01)10385609020039(17)XXXXXX(10)XXXXXXXX
- Lot Numbers
DM218001DM218002DM218003DM218004DM218005DM218006DM218020DM218025DM218034DM218035DM218036
- Amount recalled
- 49,074 devices
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
There is a potential for "No Needle Demo Units" to contain a needle.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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