Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brand Name: Rocket Product Name: Rocket 20Fg Seldinger Catheter Procedure Recalled by Rocket Medical Plc Due to IFU and device kit labeling contains misleading statements...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Rocket Medical Plc directly.
Affected Products
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 allow percutaneous insertion, supplied with connectors to allow attachment to chest drain bottle devices. Component: N/A
Quantity: 246 units
Why Was This Recalled?
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Where Was This Sold?
This product was distributed to 12 states: CO, CT, IL, ME, MA, NH, NJ, NM, OH, RI, SC, TX
About Rocket Medical Plc
Rocket Medical Plc has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report