Reported Feb 5, 2020 · Terminated
VitreQ 23G VFI Cannula-REF: CN23.D03 GTIN: 8719214221423
Vitreq Bv
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: Vitreq Bv · Seggelant-Noord 2 · Vierpolders, N/A · N/A
Is this the product you have?
- VitreQ 23G VFI Cannula-REFCN23
- D03 GTIN8719214221423
- Lot codes and dates
- All lots
- Amount recalled
- N/A
This recall covers 16 products
The agency filed one notice per product. You are reading one of them; the other 15 are below.
3 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Microscopic tears of the sterile pouch may compromise sterility
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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