Merit Custom Syringe Kit, Convenience Kit, I.R. Embolization Pack, K02-01010A, Sterile EO.
FDA Recall Z-1320-2014 · Posted 2014-04-03
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Reason for Recall
Firm Action
Root Cause
Release of Material/Component prior to receiving test results
Distribution Pattern
Worldwide Distribution - USA Nationwide in the state of WI and countries of Thailand and Hong Kong.
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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