Device recall

Z-2376-2024: OUTLOOK IV SET 15DROP W/2 CARESITE-Used with an electrically-powered infusion…

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

Key facts

Recall number (Z-number) Z-2376-2024
Recall event 94823
Product OUTLOOK IV SET 15DROP W/2 CARESITE-Used with an electrically-powered infusion pump for intravenous (IV) administration of medication. Model/Catalog Number: 354212
Product code FPA
Recalling firm B. Braun Medical, Inc.
Recall class Class II
Status Open, Classified
510(k) numbers K083723, K913661
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

Browse all FDA device recalls (products)