FDA Class II Recall Issued for American Contract System Convenience Kits
The FDA has classified a recall of American Contract System Convenience Kits as Class II due to performance specification failures in included catheters.
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The FDA has classified a recall of American Contract System Convenience Kits as Class II due to performance specification failures in included catheters.
FDA classifies recall of anterior cervical and spine packs as Class II due to potential endotoxin variability in supplied sponges.