DLP® 10060Recalls & reported problems
Medtronic, Inc. · SUCTION 10060 INTRACAR 20FR TIP 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.
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-1804-2024 · Root cause: Process control · Recall details · FDA record ↗
Other SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS devices
- DLP® 10050Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall6 reports
- DLP® 10053Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall2 reports
- DLP® 10052Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall2 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS9 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS6 reports
- DLP® 10051Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 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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