Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K041399 |
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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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Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device Rx Only Sterile Produc... | 2 | 06/04/2019 | Smiths Medical ASD Inc. |
Hypodermic Needle Pro® Edge" Safety Device with Syringe 20G x1 5mL Luer lock syringe; Reorder Numbe... | 2 | 12/30/2014 | Smiths Medical ASD, Inc. |
Hypodermic Needle Pro® Edge" Safety Device 20G x1; Reorder Number: 402010 Product Usage: The Nee... | 2 | 12/30/2014 | Smiths Medical ASD, Inc. |
Hypodermic Needle Pro® Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Numbe... | 2 | 12/30/2014 | Smiths Medical ASD, Inc. |
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