PortexRecalls & reported problems across all models
Icu Medical, Inc. · 409 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Portex models — page 5
409 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Portex A4032-18Anesthesia conduction kit1 report
- Portex 4645PGTubes, vials, systems, serum separators, blood collection1 report
- Portex 4590PGTubes, vials, systems, serum separators, blood collection1 report
- Portex A4107-25Anesthesia conduction kit1 report
- Portex A4100-17Anesthesia conduction kit1 report
- Portex A4134-17Anesthesia conduction kit1 report
- Portex A4183-17/27Anesthesia conduction kit1 report
- Portex A4197Anesthesia conduction kit1 report
- Portex 0552HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)1 death1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- 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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