Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K130581 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| REF: 126590, MEDLINE, STERILE ULTRASOUND GEL, 0.70 FL oz. (20 mL), QTY: 50, STERILER, CE 2292 | 2 | 01/20/2024 |
FEI # 3009482034 Turkuaz Saglik Hizmetleri Medikal Temizlik Kim. Ur. San. ve Tic. A.S. |
| ASG-001; Ultrasound gel | 2 | 09/09/2023 |
FEI # 1037885 Advance Medical Designs, Inc. |
| 50-GEL20; Ultrasound gel | 2 | 09/09/2023 |
FEI # 1037885 Advance Medical Designs, Inc. |
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