[Recalled] 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 st
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| 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 |
|---|---|
| Brand / manufacturer | Rocket Medical Plc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0955-2026 |
| Country of notice | United Kingdom |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 07 November 2025 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
This Class II recall concerns device products distributed in United Kingdom and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Rocket Medical Plc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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