Manufacturer
112 recalls in our database name Carefusion 2200 Inc as the manufacturing or recalling firm.
Of the 112 recalls from Carefusion 2200 Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2 (2%) are Severe.
Which agencies issued them
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Carefusion 2200 Inc is recalling 790 units of Jamshidi Needle Biopsy devices because the integrity of the sterile packaging is potentially compromised.
Carefusion 2200 Inc is recalling Broselow/Hinkle Pediatric Emergency System Oxygen Delivery Modules because they contain an 8 cm airway instead of the labeled 5 cm size.
Carefusion 2200 Inc is recalling Broselow Pediatric Emergency System pouches because the PINK/RED Oxygen Delivery Module contains an 8 cm airway instead of the labeled 5 cm size.
BD is recalling specific Diamond-Flex Circular Retractors because a weld failure could cause wire protrusion, potentially damaging tissue or organs during use.
CareFusion is recalling approximately 318,280 heated infant breathing circuits due to a regulatory compliance risk involving a material change to the gas pathway.
CareFusion is recalling surgical scrub brushes because the available iodine content is lower than stated on the label.
CareFusion is recalling surgical scrub brushes because the available iodine content is lower than stated on the label.
CareFusion is recalling Thoracentesis and Safe-T Thoracentesis Trays because the included catheters may occlude, potentially delaying medical procedures and causing patient complications.
CareFusion is recalling 14,112 manual resuscitators because a blocked oxygen connector may prevent supplemental oxygen from reaching the patient.
CareFusion is recalling AirLife Infant Patient Y Connectors because the adapter may crack, causing a leak that reduces the air volume delivered to ventilated patients.
CareFusion is recalling AirLife infant breathing circuits because a Y adapter may crack, causing a leak that reduces air delivery to ventilated patients.
CareFusion is recalling AirLife Isothermal Breathing Circuits because the Y adapter may crack, causing a leak that reduces the air volume delivered to ventilated patients.