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

Recall Z-2432-2019 — EXACTAMED Oral Dispensers, 5mL, AMBER: PHARMACY PACK, REF H9388505, x500 PHARMACY PACK, REF H9388105, x100 COST CONTAINMENT, REF H93884205, x1500

U.S. FDA — Device Enforcement · United States · 2019-06-27 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2432-2019
Date of alert
2019-06-27
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Reported risk: EXACTAMED 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 10 mL oral dispensers.
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.

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