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CareFusion 303, Inc. recalls BD Pyxis" Anesthesia Station ES, REF: 327
Recalled June 5, 2024 · FDA recall Z-1931-2024 · CareFusion 303
Hazard
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire. · FDA Class II
Units
71,569 units
Sold at
Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MP, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of South Africa, Kuwait, Qatar, Singapore, Bermuda, United Arab Emirates, Argentina, Australia, Belgium, Bahrain, Brazil, Bahamas, Canada, Chile, China, Germany, Spain, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Italy, Japan, South Korea, Lebanon, Morocco, Mexico, New Zealand, Oman, Portugal, Thailand, Taiwan.
Description
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Product
BD Pyxis" Anesthesia Station ES, REF: 327
Manufacturer(s)
CareFusion 303, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →