DeRoyal 71-C6100NSRecalls & reported problems
Deroyal Industries, Inc. · Tubing Suction Connector · Class 2
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
- Jan 31, 2025Open, Classified
Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic material, makes the assembly to a suction canister lid port difficult. This could result in inadequate suction and cause a delay in patient care.
Z-1291-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other TUBE, ASPIRATING, FLEXIBLE, CONNECTING devices
- DeRoyal 71-C506Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall4 reports
- DeRoyal 71-C512Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall2 reports
- DeRoyal 71-C520Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall1 report
- DeRoyal 71-C510Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C501Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C5100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C7100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- CONMED 0037860Conmed Corporation · TUBE, ASPIRATING, FLEXIBLE, CONNECTING20 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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