Medical Device Recalls
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41 to 50 of 84 Results
510(K) Number: K113046 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| ProScreen 12 Panel Cup w/Adult., Item No. PSCupA-12M ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 12 Panel Dip Card, Item No. PSD-12BUP ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 5 Panel Dip Card, Item No. PSD-12BUP ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB300 ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 6 Panel Cassette w/Adult (AU), Item No. PSPA-6MBAU ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB,... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 6 Panel Dip Card w/Adult (AU), Item No. PSDA-6MBAU ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 6 Panel Dip Drug Screen, Item No. PSD-6BUPO3 ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 7 Panel Dip Card, Item No. PSD-7MPB, PSD-7MO, PSD-7M ... | 3 | 12/24/2015 | Ameditech Inc |
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