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

Recall Z-0122-2026 — ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 25 Ga. x 5 in. (12.7 cm) Spinal Needle with Marking and Centering Sleeve, and 19 Ga. Closed Tip PERIFIX FX Springwound Epidural Catheter. Product Code: ES1725KFX. Product Descripti

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

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0122-2026
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): 04046955899531

Reported risk: Potential for the lid of the catheter connector to be in the incorrect position.

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.

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