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Recall Observatory FDA recall evidence

Device product

NxStage Cartridge Express with Speedswap, Catalog No. CAR-535. An accessory device for facilitating the removal and replacement of a flow-compromised filter during treatment of acute and chronic renal failure or fluid overload.

Z-1191-2024

January 29, 2024

Class II

Product summary

Firm
NxStage MDS Corporation
Event
Event 93886
Status
Ongoing
Classification
Class II
Quantity
693
Official record key
device-enforcement:Z-1191-2024

Official wording

Reason: Product is recalled due to reports of blood leaking or spraying from the arterial line on the cartridge.If this failure occurs, a patient may experience uncontrolled blood loss or a healthcare professional could be exposed to infectious patient blood.

Code information: UDI-DI M535CAR5350; Package DI M535CAR5355 Lots 20878001, 30978013, 30978032, 31178011, 31178019

Distribution pattern: US domestic distribution to Dialysis Centers located in AZ, CA, CO, GA, IL, IN, MA, MD, MI, MN, MO, MS, NC, NJ, NY, TN, TX, VA, WI. No international distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Product is recalled due to reports of blood leaking or spraying from the arterial line on the cartridge.If this failure occurs, a patient may experience uncontrolled blood loss or a healthcare professional could be exposed to infectious patient blood.