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ACCUPROBE®
Hologic, Inc. · Model KIT, ACCUPROBE M. KANSASII · UDI-DI 15420045506152
LQF
Prescription
1
510(k) clearances
2
Adverse events
2
Recalls
0
Facilities
Description
AccuProbe® Mycobacterium kansasii.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-12-30 | Gen-Probe Inc | This recall has been initiated following the identification of certain assay tubes that do not contain probe reagent. The affected kits may contain a combination of tubes with corr |
| 2008-12-30 | Gen-Probe Inc | This recall has been initiated following the identification of certain assay tubes that do not contain probe reagent. The affected kits may contain a combination of tubes with corr |
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