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

Recall Z-2171-2017 — 1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Systems (Part Number M8275093/5). The InfoV.A.C. and V.A.C.ULTA Negative Pressure Wound Therapy Systems are integrated wound management systems for use in acute, and extended and care settings. They are intended to create an enviro

U.S. FDA — Device Enforcement · United States · 2017-04-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2171-2017
Date of alert: 2017-04-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: KCI USA, INC.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 51020446

Reported risk: Potential sterile barrier breach

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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