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

Recall Z-0008-2020 — ExactaMix, Model: H938905, EMPTY EVA DUAL CHAMBER CONTAINER With Screw Connectors, 250 ml/ 1250 ml, Baxter - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of

U.S. FDA — Device Enforcement · United States · 2018-09-21 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0008-2020
Date of alert: 2018-09-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: The Metrix Company
Product category: device
Product type: Devices

Reported risk: Potential for leaking product

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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