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

Recall Z-1176-2025 — 3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit VIAKIT07S05/AU - V.A.C. VIA Starter Kit 65-Pack VIAKIT077D01/GB - V.A.C. VIA 7 Day Kit, Single Shipper

U.S. FDA — Device Enforcement · United States · 2025-01-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1176-2025
Date of alert: 2025-01-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: KCI USA, INC.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00849554002388

Reported risk: Due to increase in complaints related to leak alarms

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-1176-2025 — 3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit VIAKIT07S05/AU - V.A.C. VIA Starter Kit 65-Pack VIAKIT077D01/GB - V.A.C. VIA 7 Day Kit, Single Shipper

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