Reported Dec 21, 2022 · Ongoing
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection…
Cordis US Corp.
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: Cordis US Corp · 14201 Nw 60th Ave · Miami Lakes, FL · 33014-2802
Is this the product you have?
- Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
- Lot codes and dates
- UDI-DI(01)2070532064702
- Catalog Number (Lot Number)
502-100D (18068258180697441810104118111609)502-101D (180628811808130718064731180863881806653518097369180708241810262318077497)502-102D (1806099718078225180991181806288218079156181043131806473218083133181060931807250818084892181080191807405818088193181095121807642018090247)
- Amount recalled
- 16,950 units (2,915 US and 14,000 OUS)
Where it was sold
Why it was recalled
There is a potential for separation at the male connector.
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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