Z-2193-2014 Class II Terminated

Recalled by Gambro Renal Products, Incorporated — Lakewood, CO

FDA device recall Z-2193-2014 was initiated by Gambro Renal Products, Incorporated on July 18, 2014 and is designated Class II. 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. The recall status is terminated (terminated February 5, 2015). Affected quantity: 401,451.

Recall Details

Product Type
Devices
Report Date
August 20, 2014
Initiation Date
July 18, 2014
Termination Date
February 5, 2015
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
401,451

Product Description

Prismaflex TPE 2000 set, Product Number 1071441. Each set is packaged in a plastic pouch, 4 pouches per carton box

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.

Distribution Pattern

Worldwide Distribution.

Code Information

Product Number 1071441. Batch number 12A1905 to 14C1706. Expiry date 01/2015 to 03/2017.