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Recall Observatory FDA recall evidence

Device product

Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.

Z-0472-2020

October 21, 2019

Class II

Product summary

Firm
Cook Inc.
Event
Event 84125
Status
Terminated
Classification
Class II
Quantity
5
Official record key
device-enforcement:Z-0472-2020

Official wording

Reason: The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.

Code information: REF (RPN): HNB5.0-38-100-P-NS-AR1 REF (GPN): G10751 Lot Number: 9707476 UDI: (01)00827002107519(17)220514(10)9707476

Distribution pattern: Worldwide distribution - US Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, IL, IN, KS, LA, MA, MD, Ml, MN, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WV, and PR. Countries of AU, BE, CA, CN, CZ, DK, FR, DE, GT, HK, IT, KR, LU, MX, NL, PK, PL, ZA, ES, SE, CH, TW, and GB.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The potential compromise of the sterility of products from an undersealed chevron in the packaging pouches of Torcon NB Advantage Catheters.