Abbott GmbH Recall 94205
Description: ARCHITECT Anti-HCV Reagent Kit, List Numbers: a) 1L79-25, b) 1L79-35
Abbott GmbH Recall 94205 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | Z-1479-2024 |
Event ID | 94205 |
Event Description | ARCHITECT Anti-HCV Reagent Kit, List Numbers: a) 1L79-25, b) 1L79-35 |
Product Type | Devices |
Distribution | US Nationwide distribution. |
Quantity | 7219 units |
Recall Reason | Customer complaints were received regarding falsely elevated results for some patient samples. Internal studies with customer return samples confirmed potential interactions that may lead to falsely elevated results when processed as below on the same instrument: " ARCHITECT Syphilis TP (LN 8D06) and/or ARCHITECT AdviseDx SARS-CoV-2-IgG II (LN 6S60) precedes ARCHITECT Anti-HCV testing (LN 1L79). " Alinity i Syphilis TP (LN 07P60) precedes Alinity i Anti-HCV testing (LN 08P05). |
Device Classification | 20240410 |
Device Code Info | a) 1L79-25, 00380740001414, Lot Numbers: 52011BE00, 54140BE00, 56375BE00, 58163BE00, 59194BE00; b) 1L79-35, 00380740001421, Lot Numbers: 52015BE00, 54144BE00, 56379BE00, 58167BE00, 59198BE00 |
Center Classification Date | 20240404 |
Recall Initiation Date | 20240304 |
Recalling Firm | Abbott GmbH |
Initial Notification | Letter |
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