CareFusion 303, Inc. 2024-09-25 Health serious FDA
Health · FDA · Recall #FDA-Z-3140-2024
Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system Recall
Issued September 25, 2024 · CareFusion 303, Inc.
In September 2024, CareFusion 303, Inc. recalled the Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
What you should do
- 1 Stop using Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact CareFusion 303, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- CareFusion 303, Inc.
- Category
- Health
- Recall date
- September 25, 2024
- Units affected
- Not reported
- Sold at
- Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, HI, IA, ID, IL, IN, KS
- Recall number
- FDA-Z-3140-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- CareFusion 303, Inc. has 13 recalls in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.