Anesthesia Circuit Kit Coax 1 MP02730Recalls & reported problems
Drägerwerk AG & Co. KGaA · Class 1
- 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.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Apr 17, 2023Terminated
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Z-1452-2023 · Root cause: Process control · FDA record ↗
Other Anesthesia Breathing Circuit Kit (Adult & Pediatric) devices
- Anesthesia Circuit Kit Coax HEPA MP17102Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- AirLife™ 2K8000Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- AirLife™ 2K8001Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- AirLife™ AH265Airlife · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- AirLife™ AH265Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- Anesthesia Circuit Kit Coax 3 MP02732Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- Anesthesia Circuit Kit Flex 6 MP02744Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)6 reports
- AirLife™ AH202Airlife · Anesthesia breathing circuit kit (adult & pediatric)5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.