Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K130136 |
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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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Disposable Subdermal Needle Electrode, Pt/lr, 12 x 0.40mm, product number TE/S46/638, 25 needles per... | 2 | 09/12/2022 | Technomed Europe |
Disposable Subdermal Needle Electrode, Corkscrew, Single Use, Sterile; Model Numbers TE/S50715-001-C... | 2 | 01/07/2022 | Technomed Europe |
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