Z-0603-2021 Class I Terminated
Recalled by Cook Inc.
— Bloomington, IN
FDA device recall Z-0603-2021 was initiated by Cook Inc. on Nov 24, 2020 and is designated Class I. Reason for recall: There is an increased likelihood of the introducer sheath separating at the proximal bond site. If separation occurs during use, it could result in life-threatening adverse events. The potential… The recall status is terminated (terminated Sep 7, 2022). Affected quantity: 3797.
Recall Details
- Product Type
- Devices
- Report Date
- Dec 30, 2020
- Initiation Date
- Nov 24, 2020
- Termination Date
- Sep 7, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3797
Product Description
Flexor Check-Flo Introducer, RPN KCFW-7.0-35-55-RB-HFANL1-HC, Order Number G49043 Flexor Introducers and Guiding Sheaths are intended to introduce therapeutic or diagnostic devices into the vasculature, excluding coronary and neuro vasculature.
Reason for Recall
There is an increased likelihood of the introducer sheath separating at the proximal bond site. If separation occurs during use, it could result in life-threatening adverse events. The potential adverse events that may occur include, but are not limited to increased procedural time, intervention to retrieve a separated segment, embolization occluding blood flow to a vital organ, vessel injury, and hemorrhage.
Distribution Pattern
US Nationwide Distribution including states of: AK, CT, IA, LA, MO, NH, OK, TN, WI, AL, DC, ID, MA, MS, NJ, OR, TX, WV, AR, DE, IL, MD, MT, NM, PA, UT, WY, AZ, FL, IN, ME, NC, NV, RI, VA, CA, GA, KS, MI, ND, NY, SC, VT, CO, HI, KY, MN, NE, OH, SD, WA and Global Distribution to: AU, SG, Austria, Belgium, Canary Islands, CN, Czech Republic, Denmark, Egypt, Finland, France, Germany, Greece, Hong Kong, Hungary, Ireland, Italy, KR, Latvia, Lithuania, MY, Morocco, Netherlands, Norway, Poland, Portugal, Reunion, Russian Federation, Saudi Arabia, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, TW, TH, and United Arabs Emirates.
Code Information
Lot Numbers: 13192055, 13192067, 13200423, 13200424, 13202961, 13202963, 13205309, 13205315, 13205323, 13205324, 13223833, 13229686, 13229687, 13231803, 13234792, 13234801, 13237654, 13243208, 13243209, 13246544, 13246548, 13249451, 13249452, 13249453, 13254617, 13254618, 13262329, 13262330, 13279085, 13281530, 13281531, 13281790, 13281791, 13286645, 13286646, 13286647, 13286648, 13286650, 13286651, 13286652, 13303358, 13303361, 13303362, 13303366, 13303367, 13303368, 13303371, 13303372, 13303373, 13303374, 13303375, 13306335, 13306336, 13319484, 13319489, 13319495, 13346087, 13349006, 13352444, 13354260, 13354261, 13354262, 13357229, 13357230, 13360411, 13360412, 13360413, 13363220, 13363221, 13366231, 13366232, 13372470, 13372491, 13380384, 13382718, 13388328, 13391161, 13398857, 13401849, 13435154, 13438159, 13449366, 13449367, 13455464, 13279081X
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0603-2021
- openFDA file date
- Oct 6, 2026
- Loaded by RegDataLab
- Oct 12, 2026
These dates say when openFDA published the data file and when RegDataLab last loaded it. FDA may have changed the recall since.