Medical Device Recalls
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31 to 40 of 86 Results
510(K) Number: K052115 |
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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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| Immutest 10 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-10M5 ... | 3 | 12/24/2015 | Ameditech Inc |
| Immutest 11 Pnl Drug Screen Cup w/ Adult, Item No. IMCA-11OP ... | 3 | 12/24/2015 | Ameditech Inc |
| Immutest 5 Pnl Drug Cup w/ Adult -waived, Item No. IMCA-5AB-W ... | 3 | 12/24/2015 | Ameditech Inc |
| Immutest 12 Panel Cup w/Adulteration, Item No. IMCA-11OP ... | 3 | 12/24/2015 | Ameditech Inc |
| ImmuTest 12 Panel Dip Card, Item No. IMD-12MO3 | 3 | 12/24/2015 | Ameditech Inc |
| ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P ... | 3 | 12/24/2015 | Ameditech Inc |
| Immutest Cup CLIA Waived w/Adulteration, Item No. IMCA-7MT-W ... | 3 | 12/24/2015 | Ameditech Inc |
| 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 |
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