FDA recall record

Rocket 18Fg Seldinger Catheter with Safety Guard recall — FDA Z-0953-2026

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

Class IIclassification
Z-0953-2026official record ID
Dec 24, 2025report date

Recall record at a glance

Official recordZ-0953-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmRocket Medical Plc
Report dateDec 24, 2025
Recall initiation dateNov 7, 2025
Quantity110 units
LocationTyne & Wear, United Kingdom

Official product description

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 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.

Why the product was 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.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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