Device recall

Z-0935-2020: Outlook Safety Infusion System Y-type Blood Set, Catalog Number 477005

FDA device recall · Class II · B. Braun Medical, Inc.

Key facts

Recall number (Z-number) Z-0935-2020
Recall event 84365
Product Outlook Safety Infusion System Y-type Blood Set, Catalog Number 477005
Product code FPA
Recalling firm B. Braun Medical, Inc.
Recall class Class II
Status Terminated
Termination date Oct 16, 2020
510(k) numbers K140311, K922637
FEI number 2523676

At a glance

  • 1–9 Linked 510(k)s
  • 10–99 Products in the same recall event
  • 1,000+ 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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