BD Pyxis(TM) Anesthesia Station 4000, REF: 338
Reported: June 5, 2024 Initiated: April 15, 2024 #Z-1932-2024
Product Description
BD Pyxis(TM) Anesthesia Station 4000, REF: 338
Reason for Recall
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Details
- Recalling Firm
- CareFusion 303, Inc.
- Units Affected
- 11,875 units
- Distribution
- 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.
- Location
- San Diego, CA
Frequently Asked Questions
What product was recalled? ▼
BD Pyxis(TM) Anesthesia Station 4000, REF: 338. Recalled by CareFusion 303, Inc.. Units affected: 11,875 units.
Why was this product recalled? ▼
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 5, 2024. Severity: Moderate. Recall number: Z-1932-2024.
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