Device recall

Z-1589-2015: 107" (272 cm) Ext Set w/2 Check Valves, MicroClave T-Connector, Clamp, Rotating…

FDA device recall · Class II · ICU Medical, Inc.

Key facts

Recall number (Z-number) Z-1589-2015
Recall event 71028
Product 107" (272 cm) Ext Set w/2 Check Valves, MicroClave T-Connector, Clamp, Rotating Luer, Non-DEHP Tubing, Item No. B33041 Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.
Product code FMG
Recalling firm ICU Medical, Inc.
Recall class Class II
Status Terminated
Termination date Nov 24, 2015
510(k) numbers K964435
FEI number 2025816

At a glance

  • 1–9 Linked 510(k)s
  • 1–9 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

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