Medical Device Recalls
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51 to 60 of 79 Results
510(K) Number: K113501 |
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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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| Micro Screen 6 Panel Cup with Adult (AU), Item No. MSCA-6MBAU ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 10 Drug Panel Cassette Test, Item No. PSP-10PPX ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 10 Panel Cup, Item No. PSCup-10M ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScProScreen 10 Panel Cup with Adulterants, Item No. PSCupA-10AM ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 10 Panel Dip Card, Item No. PSD-10MOX, PSD-10MOB, PSD-10MMO300 ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 10 Panel Dip Card w/Adult, Item No. PSDA-10MO, PSDA-10MMO300, PSDA-10PPX, PSDA-10BUP, PSD... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 12 Drug Cup w/Adulteration, Item No. PSCupA-12TBU ... | 3 | 12/24/2015 | Ameditech Inc |
| 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 |
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