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

Recall Z-2799-2018 — 30 cm (12") PUR Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, 2 NanoClave, Rotating Luer a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system.

U.S. FDA — Device Enforcement · Mexico · 2018-03-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2799-2018
Date of alert: 2018-03-01
Country / jurisdiction: Mexico
Risk level: Class II
Risk type: recall
Brand: ICU Medical de Mexico, S.A. de C.V.
Product category: device
Product type: Devices

Reported risk: ICU Medical is expanding the scope of their previously initiated recall to include additional I.V. Administration Sets with NanoClave manifold due to the potential to develop a leak or for separation between the female luer and the NanoClave manifold.

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-2799-2018 — 30 cm (12") PUR Bifuse Ext Set w/3-Port NanoClave Manifold, Check Valve, 2 NanoClave, Rotating Luer a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system.

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