Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0951-2026 — 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 manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplied with a procedure p

U.S. FDA — Device Enforcement · United Kingdom · 2025-11-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0951-2026
Date of alert
2025-11-07
Country / jurisdiction
United Kingdom
Risk level
Class II
Risk type
recall
Brand
Rocket Medical Plc
Product category
device
Product type
Devices
Reported risk: IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.