Reported Aug 27, 2014 · Terminated
Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 30 cm Infusion Pattern, Catalog No./REF 12401808, Product No.…
Angiodynamics, Inc.
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: Angiodynamics, Inc. · 603 Queensbury Ave · Queensbury, NY · 12804-7619
Is this the product you have?
Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE5F x 90 cm x 30 cm Infusion PatternCatalog No./REF 12401808Product No. H787124018085STERILE -- AngioDynamics603 Queensbury AvenueQueensburyNY 12804
- Lot codes and dates
- Lot 4731641 (exp. date 31-Mar-17)
- Amount recalled
- Domestic: 81 units; Foreign: 13 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire have the potential to contain an incorrect sized guidewire (too long).
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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