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Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-18-PK Sof
Recalled December 24, 2025 · FDA recall Z-0952-2026 · Rocket Medical
Hazard
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use. · FDA Class II
Units
630 units
Sold at
Domestic: CO, CT, IL, MA, ME, NH, NJ, NM, OH, RI, SC, TX; International: UAE, Austria, Australia, Canada, Germany, Denmark, Finland, France, United Kingdom, Greece, Hong Kong, Ireland, Israel, India, Italy, Jersey, Kenya, Sri Lanka, Malta, Netherlands, Norway, New Zealand, Portugal, Saudi Arabia, Singapore, Slovenia, South Africa
Description
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Product
Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-18-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
Manufacturer(s)
Rocket Medical Plc
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →