Recall
Get alerts

rocket medical plc

6 recalls on record

Get alerts
R
Rocket Medical Plc — Brand Name: Rocket Product Name: Rocket 16Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54549-16-PK Software Version: N/A Product Description: Chest tube manufac

IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

R
Rocket Medical Plc — 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 manufac

IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

R
Rocket Medical Plc — Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-12-SG Software Version: N/A Product Description: Chest tube manu

IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

R
Rocket Medical Plc — 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 manufac

IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

R
Rocket Medical Plc — Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray Model/Catalog Number: R54544-12-PK Product Description: Chest tube manufactured from PVC, with fe

IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.

R
Rocket Medical Plc — Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-18-SG Software Version: N/A Product Description: Chest tube manu

IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.