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

Recall Z-1168-2025 — Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/Catalog Number: 31815 Software Version: N/A Product Description: MediHoney¿ Gel with Active Leptospermum Honey is a moist dressing made of Active Leptospermum Honey in combination with gelling agents. The gelling

U.S. FDA — Device Enforcement · United States · 2025-01-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1168-2025
Date of alert: 2025-01-10
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Integra LifeSciences Corp.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10381780486886

Reported risk: Potential that the induction seal is not completely sealed to the device tube packaging.

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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