Reported Aug 25, 2021 · Ongoing
DELTAVEN FASTFLASH, Safety I.V. Catheter in Pur with closed system
Delta Med SpA
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: Delta Med SpA · Via Guido Rossa 20 · Viadana, N/A · N/A
Is this the product you have?
DELTAVEN FASTFLASH, Safety I.V. Catheter in Pur with closed system
24 of 24 products
| Model / number | Product as published |
|---|---|
3814773 | — |
3835773 | — |
3825773 | — |
3837773 | — |
3846773 | — |
3831473 | — |
3842473 | — |
3821473 | — |
3832473 | — |
3833473 | — |
3821573 | — |
3831573 | — |
3833573 | — |
3824773 | — |
3804773 | — |
3845773 | — |
3811473 | — |
3836773 | — |
3843473 | — |
3800473 | — |
- Amount recalled
- 229,320 units
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
Why it was recalled
Problems related to the sterilization of the medical devices; possible missing sterility of the medical device
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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