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Cook Incorporated recalls Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular a
Recalled April 24, 2024 · FDA recall Z-1526-2024 · Cook Incorporated
Hazard
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility · FDA Class II
Units
55 units
Sold at
Worldwide distribution - US Nationwide and the countries of AT, AU, BR, CA, CH, DE, ES, GB, HK, IE, IL, IN, IT, NZ, SG.
Description
Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility
Product
Trocar Needle - Used for dilating puncture sites or catheter tracts for percutaneous placement of devices for vascular and non-vascular applications such as in the venous, arterial, biliary and renal system REFERENCE PART NUMBER (RPN): DTN-18-20.0 ORDER NUMBER (GPN): G01377
Manufacturer(s)
Cook Incorporated
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →