Z-2202-2014 Class II Terminated
FDA device recall Z-2202-2014 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 M100. Product number 106697. 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
Prismaflex M100. Product number 106697. Batch number 12A0401G to 14C2802G. Expiry 01/2014 to 03/2016