fda
2 records
FDA Recall: Iradimed Corporation — Class II
20121205
Iradimed Corporation is recalling MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extension Set, Lot Code LBG001 because a section of the device | Product: The brand name is MRidium Series 1000 ...
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FDA Device Recall: The brand name is MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extensio
2012-12-05
Class II — Iradimed Corporation is recalling MRidium Series 1000 MR Infusion Sets, Type 1058 MR IV Extension Set, Lot Code LBG001 because a section of the device does not meet specifications.
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SEC EDGAR
1 records
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