MLAClass I
Dna Probe, Yeast
Microbiology · 21 CFR 866.2660
MDR events190All time
Recalls2All time
Registered firms6Currently listed
510(k) clearances2All time
Recent MDR events
190 adverse event reports on file
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTOct 9, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00643
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTOct 9, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00644
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTSep 19, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00639
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTAug 1, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00137
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTJul 30, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00227
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTJul 30, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00217
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTJul 30, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00214
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTJul 30, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00228
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTJul 30, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00216
- BD AFFIRM¿ VPIII MICROBIAL IDENTIFICATION TESTJul 30, 2025MalfunctionBecton Dickinson Caribe Ltd.2647876-2025-00225
Event type breakdown
Malfunction184
Injury6
Recalls
2 recall events for this product code
- Becton Dickinson & Co.TerminatedFeb 27, 2017
BD AffirM VPIII Microbial Identification Test
BD has confirmed that a portion of tests associated with the affected lots( 446252 and 446257 ) of product may exhibit blue speckles or fibers on the beads and cards, as shown below. This issue would result in an invalid test, as described in the package insert.
Z-1394-2017 · View FDA record ↗ - Becton Dickinson & Co.TerminatedJul 26, 2013
BD Affirm VPIII Microbial Identification Tests, packaged in kits, 120 test\kit, Catalog # 446257 and 24 test\kit, Catalog # 446252; kits are labeled in part ***
In vitro diagnostic test kit may exhibit invalid internal negative control results.
Z-1812-2013 · View FDA record ↗
Registered firms
6 firms currently registered for this product code
510(k) clearances
2 clearances for this product code