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

PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and PERIFIX FX Springwound Catheter - 19 Ga. Closed Tip. Product Code: CE17TBFC. Product description: CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY. — recall Z-0114-2026

U.S. FDA — Device Enforcement · United States · 2025-09-18 · Class II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0114-2026
Date of alert
2025-09-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
B BRAUN MEDICAL INC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
4046964177187
Reported risk: Potential for the lid of the catheter connector to be in the incorrect position.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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.