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Recall Observatory FDA recall evidence

Device product

Dilator With AQ Hydrophilic Coating - Intended to be 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 systems. REFERENCE PART NUMBER (RPN)/ORDER NUMBER (GPN): 1) JCD10.0-38-20-HC G10207 2) JCD14.0-38-20-HC G10293 3) JCD16.0-38-20-HC G10206 4) JCD6.0-38-20-HC G10285 5) JCD8.0-38-20-HC G10289

Z-1531-2024

March 01, 2024

Class II

Product summary

Firm
Cook Incorporated
Event
Event 94196
Status
Ongoing
Classification
Class II
Quantity
1,493 units
Official record key
device-enforcement:Z-1531-2024

Official wording

Reason: Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Code information: Ref. Number/UDI-DI/Lot Numbers: 1) JCD10.0-38-20-HC (01)00827002102071(17) 15794369 2) JCD14.0-38-20-HC (01)00827002102934(17) 15778297, 15787264 3) JCD16.0-38-20-HC (01)00827002102064(17) 15794375 4)JCD6.0-38-20-HC (01)00827002102859(17) NS15808469 5) JCD8.0-38-20-HC (01)00827002102897(17) 15761259

Distribution pattern: Worldwide distribution - US Nationwide and the countries of AT, AU, BR, CA, CH, DE, ES, GB, HK, IE, IL, IN, IT, NZ, SG.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility