Reported Sep 10, 2025 · Ongoing
DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110
Medtronic Perfusion Systems
High riskUsing this product could cause serious injury, illness or death — stop using it now.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: Medtronic Perfusion Systems · 7611 Northland Dr N · Brooklyn Park, MN · 55428-1088
Is this the product you have?
- DLP Left Heart Vent Catheter Malleable body and vented connector, SUCTION 12110 LV VENT 10FR, Model Number 12110
- Lot codes and dates
- UDI-DI
2064316988067600643169880672006739781764680076300094643220763000946436
- Serial Numbers
101 of 101 codes
202312070820231207082023120709202312071020231207112023120712202312104120231210412023121042202401120320240112032024011204202402013520240201362024020137202402013820240201382024020139202402014020240201412024020141202402047120240204722024020473202402047420240204742024020474202402047520240204752024020475202402080620240208062024020806202403035920240303602024030360202403036120240303612024030361202403083320240308332024030834202403083420240308352024030835202403108820240310882024050074202405007520240500762024050403202405040420240507612024050762202405076320240507632024051075202405107620240512652024060283
- UDI-DI
- Amount recalled
- 41200 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
The catheters may not retain their shape.
Using this product could cause serious injury, illness or death — stop using it now.
Want the full recall guide?
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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