Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
Reported: April 24, 2019 Initiated: February 7, 2019 #Z-1198-2019
Product Description
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
Reason for Recall
Frayed pieces of the mounting card being inside the primary packaging.
Details
- Recalling Firm
- Cordis Corporation
- Units Affected
- 23481
- Distribution
- Worldwide Distribution - US Nationwide in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, Puerto Rico and Guam Singapore and Canada
- Location
- Miami Lakes, FL
Frequently Asked Questions
What product was recalled? ▼
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.. Recalled by Cordis Corporation. Units affected: 23481.
Why was this product recalled? ▼
Frayed pieces of the mounting card being inside the primary packaging.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 24, 2019. Severity: Low. Recall number: Z-1198-2019.
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