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Cordis US Corp recalls Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for inject
Recalled December 21, 2022 · FDA recall Z-0720-2023 · Cordis US
Hazard
There is a potential for separation at the male connector. · FDA Class II
Units
16,950 units (2,915 US and 14,000 OUS)
Sold at
Nationwide distribution to AZ, CA, DC, FL, GA, KY, LA, MD, MS, NY, OH, TX, WV, WY and PR. International distribution to Japan, Korea, Republic of, United Arab Emirates, Austria, Belgium, Czech Republic, Germany, Spain, France, United Kingdom, Iceland, Ireland, Israel, Netherlands, Portugal, Russia.
Description
There is a potential for separation at the male connector.
Product
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection into the patient.
Manufacturer(s)
Cordis US Corp
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →