Device recall

Z-0955-2026: Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Tray…

FDA device recall · Class II · Rocket Medical Plc

Key facts

Recall number (Z-number) Z-0955-2026
Recall event 97994
Product Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-20-PK Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure pack to…
Product code GBX
Recalling firm Rocket Medical Plc
Recall class Class II
Status Open, Classified
FEI number 3002808026

At a glance

  • None 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

Browse all FDA device recalls (products)