Home › Intersurgical Incorporated › 22MM COMPACT BS WITH 3L BAG LUER ELBOW MONITORING LINE ANAES FACE MASK AND HMEF
22MM COMPACT BS WITH 3L BAG LUER ELBOW MONITORING LINE ANAES FACE MASK AND HMEF
Intersurgical Incorporated · Model 2158010 · UDI-DI 05030267160228
OFP
Prescription
0
510(k) clearances
104
Adverse events (2 deaths)
33
Recalls
50
Facilities
Description
22MM COMPACT BREATHING SYSTEM WITH 3L BAG, LUER ELBOW, MONITORING LINE, ANAESTHETIC FACE MASK AND HMEF 3.0M
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-03-12 | Draeger, Inc. | The potential for cracks forming in the breathing circuit hose. |
| 2025-03-12 | Draeger, Inc. | The potential for cracks forming in the breathing circuit hose. |
| 2025-03-12 | Draeger, Inc. | The potential for cracks forming in the breathing circuit hose. |
| 2025-03-12 | Draeger, Inc. | The potential for cracks forming in the breathing circuit hose. |
| 2025-03-12 | Draeger, Inc. | The potential for cracks forming in the breathing circuit hose. |
| 2021-01-29 | Draeger Medical, Inc. | Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the patient. |
| 2021-01-29 | Draeger Medical, Inc. | Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the patient. |
| 2021-01-29 | Draeger Medical, Inc. | Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the patient. |
| 2021-01-29 | Draeger Medical, Inc. | Y-piece may become detached from the ventilation hose either before or during the ventilation process, a leak will be caused that can hinder ventilation of the patient. |
| 2020-11-11 | Intersurgical Inc | The device was assembled with the incorrect exhalation port which can cause gas leakage. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
