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

Recall Z-1363-2026 — MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum Honey provides a moist environment conducive to wound healing and is indicated for light to moderately exuding wounds.

U.S. FDA — Device Enforcement · United States · 2026-01-16 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1363-2026
Date of alert: 2026-01-16
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Integra LifeSciences Corp. (NeuroSciences)
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10381780486978

Reported risk: Potential packaging failures, which could lead to a breach in the sterile barrier.

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.

Recall Z-1363-2026 — MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: (1) 31805, (2) 31815. MediHoney Gel dressing with Active Leptospermum Honey provides a moist environment conducive to wound healing and is indicated for light to moderately exuding wounds.

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