WalkMed Infusion Triton 90" 20 drop IV Administration Set with Needlefree Y-site and 0.22 Intended use: Intravascular Administration Set
FDA Recall Z-1321-2011 · Posted 2011-02-16
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Reason for Recall
Firm Action
Root Cause
Vendor change control
Distribution Pattern
Nationwide Distribution: USA including states of: CO, IA, OH, MA, MD, MO, NY, FL, SC, FL, and VA.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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