Device recall

Z-0329-2010: 32CM ALTA EXCHANGE Model: AL27SH32 XP ALTA EXCHANGE KIT 15.5 Fr polyurethane…

FDA device recall · Class II · Spire Biomedical, Inc.

Key facts

Recall number (Z-number) Z-0329-2010
Recall event 53605
Product 32CM ALTA EXCHANGE Model: AL27SH32 XP ALTA EXCHANGE KIT 15.5 Fr polyurethane twin lumen fixed tip hemodialysis catheter, cuff and side holes for chronic hemodialysis and apheresis. Latex free
Product code MSD
Recalling firm Spire Biomedical, Inc.
Recall class Class II
Status Terminated
Termination date Jun 9, 2010
510(k) numbers K032061, K040509, K042858, K060155, K063431, K063441
FEI number 1000159376

At a glance

  • 1–9 Linked 510(k)s
  • 10–99 Products in the same recall event
  • 100–999 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

Browse all FDA device recalls (products)