Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K003712 |
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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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Non-Sterile Double DIN to DIN "Y" Connector, Product Usage: Extension for connecting hemodialysis... | 2 | 03/24/2017 | Molded Products Inc |
Sterile Access & Return Line Set, 36" Length, Part # UM-872-36. Intended for use with medically... | 2 | 03/18/2013 | Molded Products Inc |
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