Medical Device Recalls
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51 to 60 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 8 Panel Dip Card, Item No. PSD-8P ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300 ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300 ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen CLIA Waived Cup with 6 Drugs, Item No. PSCup-6BO-W ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen CLIA Waived Cup with 8 Drug, Item No. PSCup-8P-W ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen CLIA Wvd 12 Panel Cup w/Adult., Item No. PSCupA-12M-W ... | 3 | 12/24/2015 | Ameditech Inc |
| ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W ... | 3 | 12/24/2015 | Ameditech Inc |
| RealityCHECK Tilt Cup 12 Panel + Adult, Item No. RC12TCA ... | 3 | 12/24/2015 | Ameditech Inc |
| THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU ... | 3 | 12/24/2015 | Ameditech Inc |
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