PrisMARS Kit (component of MARS Treatment Kit Type 1115/1 PrisMARS US), 1 MARS Treatment Kit per carton box, Product Num
FDA device recall Z-2206-2014 · posted 2014-08-13 · Terminated
Recall details
- Recalling firm
- Gambro Renal Products, Incorporated
- Reason for recall
- Gambro initiated a field action on the Prisma and Prismaflex sets due to breakages of connectors resulting in leakage of liquid or blood.
- Action taken
- Gambro sent an Urgent Field Safety Notice dated July 18, 2014 to all end-users. A Customer Reply Form was attached to the notice for customers to complete and return.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- FLD
- Quantity affected
- 401,451
- Distribution
- Worldwide Distribution.
- Date initiated
- 2014-07-18
- Date posted
- 2014-08-13
- Date terminated
- 2015-02-05
- Location
- Lakewood, CO
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