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

Recall Z-1913-2026 — FLEXTIP PLUS EPIDURAL CATHETER;FLEXBLOCK CONTINOUS PERIPHERAL NERVE BLOCK CATHETER KIT/SET REF ASK-05502-BSM UDI code: (01)10801902209853(17)270831(11)251210(10)33F25K0409 The Arrow Epidural Catheter kit permits access to the epidural space for administration of epidural anesthetic. The epidura

U.S. FDA — Device Enforcement · United States · 2026-03-11 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1913-2026
Date of alert: 2026-03-11
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: ARROW INTERNATIONAL, LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10801902209853

Reported risk: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

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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