Adaptors/Connectors S6411PRecalls & reported problems
Westmed, Inc. · Flex Extender, 5.2" x 15mm OD x 15mm ID · Class 1
Data updated Oct 18, 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 18, 2026.
Recalls naming this device
- Sep 27, 2024Class IIOpen, Classified
Due to connector within the circuit flex extender not meeting specifications resulting in a low connection force and as a result, the connector may leak or disconnect and may cause life threating conditions or death.
Z-0263-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Connector, Airway (Extension) devices
- Flex Extenders 7-5132Westmed, Inc. · Connector, Airway (Extension)1 recall18 reports
- ErgoStar CM 55 MP01855Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall10 reports
- ErgoStar CM 45 MP01845Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- ErgoStar CM 40 MP01840Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- Omnistream 011401Oridion Medical 1987 Ltd. · CONNECTOR, AIRWAY (EXTENSION)1 recall0 reports
- ErgoStar CM 60 MP01860Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall0 reports
- Portex 66-1991Icu Medical, Inc. · CONNECTOR, AIRWAY (EXTENSION)8 reports
- AirLife 004081Vyaire Medical, Inc. · Connector, Airway (Extension)4 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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