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Recall Observatory FDA recall evidence

Device product

PrisMARS Kit (component of MARS Treatment Kit Type 1115/1 PrisMARS US), 1 MARS Treatment Kit per carton box, Product Number 800480, Batch

Z-2206-2014

July 18, 2014

Class II

Product summary

Firm
Gambro Renal Products, Incorporated
Event
Event 68788
Status
Terminated
Classification
Class II
Quantity
401,451
Official record key
device-enforcement:Z-2206-2014

Official wording

Reason: Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.

Code information: Model Number MARS Treatment Kit Type 1115/1 PrisMARS US, Batch 0000017412 - 0000019827, Expiry Date 06/2014 to 05/2016

Distribution pattern: Worldwide Distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.