DLP® 12220Recalls & reported problems
Medtronic, Inc. · SUCTION 12220 LV VENT 20FR SIL 20PK 17L · Class 2
All models of DLP (151)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
2 other recalls cover devices cleared under the same FDA submission (K834352); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Mar 19, 2024Open, Classified
Potential for unsealed sterile packing.
Z-1797-2024 · Root cause: Process control · Recall details · FDA record ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K834352. One submission often covers many models, so check the product and lot details in each record.
- Z-2504-2021 · Aug 24, 2021 · Open, ClassifiedDLP Left Heart Vent Catheters, 16 FR. Sterile, Rx Only
- Z-2505-2021 · Aug 24, 2021 · Open, ClassifiedDLP Left Heart Vent Catheters, 18 FR. Sterile, Rx Only
Other CATHETER, STEERABLE devices
- FARADRIVE™ M004PF21M402Boston Scientific Corporation · CATHETER, STEERABLE1 recall15 deaths2,303 reports
- MITRACLIP SGC0701Abbott Vascular Inc. · CATHETER, STEERABLE17 deaths963 reports
- STEERABLE GUIDE CATHETER SGC0301Abbott Vascular Inc. · CATHETER, STEERABLE5 deaths389 reports
- FlexCath Advance™ 4FC12Medtronic, Inc. · CATHETER, STEERABLE6 deaths167 reports
- FlexCath Contour™ 10FCC13Medtronic, Inc. · CATHETER, STEERABLE2 deaths115 reports
- FlexCath Advance™ 4FC12Medtronic, Inc. · CATHETER, STEERABLE4 deaths61 reports
- FlexCath Advance™ 4FC12Medtronic, Inc. · CATHETER, STEERABLE4 deaths60 reports
- FlexCath Advance™ 4FC12Medtronic, Inc. · CATHETER, STEERABLE59 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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