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Recall Observatory FDA recall evidence

Device product

Prismaflex Control Unit, software versions below 7.21

Z-0277-2020

October 04, 2019

Class II

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 83852
Status
Ongoing
Classification
Class II
Quantity
986 units
Official record key
device-enforcement:Z-0277-2020

Official wording

Reason: Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.

Code information: Product Code: 113081; All Lot numbers; GTIN: 07332414105266

Distribution pattern: Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY. International distribution to Australia, Bangladesh, Brunei, China, Hongkong, Indonesia, India, Japan, New Zealand, Taiwan, Korea, Singapore, Malaysia, Macau, Thailand, Vietnam, Canada, Argentina, Costa Rica, Cuba, Dominican Republic, Haiti, Barbados, Venezuela, St. Kitts, and EMEA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Communication error alarms may result in interruption of therapy, delay in therapy, or blood loss due to non-restitution of blood in the extracorporeal circuit.