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

Recall Z-1365-2026 — Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment, which has shown to be conducive to wound healing. Intended for minor scalds & burns, minor cuts, lacerations & minor abrasions.

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-1365-2026
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): 00050428452547

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-1365-2026 — Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment, which has shown to be conducive to wound healing. Intended for minor scalds & burns, minor cuts, lacerations & minor abrasions.

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