Device recall

Z-2598-2014: Merci Retriever Intended to restore blood flow in the neurovasculature by…

FDA device recall · Class II · Concentric Medical Inc

Key facts

Recall number (Z-number) Z-2598-2014
Recall event 69119
Product Merci Retriever Intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stoke. Merci Retrievers are also indicated for use in the retrieval of foreign bodies misplaced during interventional radiological procedures in the neuro, peripheral and…
Product code NRY
Recalling firm Concentric Medical Inc
Recall class Class II
Status Terminated
Termination date Oct 29, 2014
510(k) numbers K082034
FEI number 3003271051

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 Products in the same recall event
  • 10–99 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

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