Medical Device Recalls
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1 result found
510(K) Number: K051436 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Pre Isotonic Personal Lubricant labeled PRE' Patient Lubricant. Product is used to lubricate vulv... | 2 | 01/23/2009 | INGfertility, LLC |
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