Reported Apr 24, 2019 · Terminated

Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for…

Cordis Corporation

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cordis Corporation · 14201 NW 60th Ave · Miami Lakes, FL · 33014-2802

Cordis Vista Brite Tip &
Androit Guiding Catheters Product UsageThe guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems

Lot codes and dates: Lot Number Exp. Date
346 of 346 codes
17744955
12/31/2020
17750783
12/31/2020
17757121
1/31/2021
17735533
10/31/2020
17735534
10/31/2020
17744429
12/31/2020
17744430
12/31/2020
17750785
12/31/2020
17757116
1/31/2021
17748743
12/31/2020
17750476
12/31/2020
17755096
1/31/2021
17757122
1/31/2021
17753002
12/31/2020
17779364
4/30/2021
17815946
9/30/2021
17805148
7/31/2021
17815949
9/30/2021
17753959
1/31/2021
17746022
12/31/2020
17762925
2/28/2021
17733016
10/31/2020
17747583
12/31/2020
17749800
12/31/2020
17752698
12/31/2020
17767925
2/28/2021
17769354
3/31/2021
17771053
3/31/2021
17772929
4/30/2021
17722360
9/30/2020
Amount recalled: 23481

Frayed pieces of the mounting card being inside the primary packaging.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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22 in total.