co_sos
1 records
fda
15 records
FDA Recall: Draeger, Inc. — Class I
20260610
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation du | Product: Atlan A350XL. Model Number: 8621600. ...
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FDA Recall: Draeger, Inc. — Class I
20251231
A certain component of affected devices was not delivered within specification and contained impurities. | Product: Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
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FDA Recall: Draeger, Inc. — Class I
20251008
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use. | Product: Brand Name: Atlan Product Name: Atlan A350 Model/...
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FDA Recall: Draeger, Inc. — Class I
20250806
Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters. | Product: SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
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FDA Device Recall: Draeger Vapor 2000. Unheated, calibrated anesthetic vaporizer.
2025-12-31
Class I — A certain component of affected devices was not delivered within specification and contained impurities.
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FDA Device Recall: ErgoStar CM 60, Model/Catalog Number: MP01860, Airway connector for cond
2025-12-17
Class I — Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
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FDA Device Recall: ErgoStar CM 45, Model/Catalog Number: MP01845, Airway connector for condu
2025-12-17
Class I — Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
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FDA Device Recall: ErgoStar CM 40 Model/Catalog Number: MP01840 Airway connector for conducti
2025-12-17
Class I — Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
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FDA Device Recall: Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Soft
2025-10-08
Class I — The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
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FDA Device Recall: Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 So
2025-10-08
Class I — The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
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FDA Device Recall: SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
2025-08-06
Class I — Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
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FDA Device Recall: SafeStar 55 Plus Filter. Bidirectionally breathing system filter.
2025-08-06
Class I — Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
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FDA Device Recall: SafeStar 60A Plus Filter. Bidirectionally breathing system filter.
2025-08-06
Class I — Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.
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FDA Device Recall: Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP0
2025-04-09
Class I — The potential for cracks forming in the breathing circuit hose.
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FDA Device Recall: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1
2025-04-09
Class I — The potential for cracks forming in the breathing circuit hose.
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ny_corps
1 records
NY Corp: DRAEGER, INC.
1996-07-17
FOREIGN BUSINESS CORPORATION | County: New York | Jurisdiction: Pennsylvania
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