Novadaq Technologies recalls
Novadaq Technologies has 7 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 4 Oct 2017. The most frequent reason is sterility.
Total recalls7since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 4 Oct 2017
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 5 71%Class III 2 29%
Why novadaq technologies is recalled
Product types
By year
All novadaq technologies recalls, newest first
7 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Novadaq Spy-phi Drape, 7" x 104" recalled by Novadaq Technologies | Novadaq Technologies | Sterility | Nationwide |
| Device | CLASS II | Novadaq Spy-phi Paq Intended for use recalled by Novadaq Technologies | Novadaq Technologies | Sterility | Nationwide |
| Device | CLASS II | Novadaq Spy-phi Drape, 7" x 104" recalled by Novadaq Technologies | Novadaq Technologies | Sterility | Nationwide |
| Device | CLASS II | Sterile Drape, SK6000 PAQ drape pouch (for use recalled | Novadaq Technologies | Sterility | FL, MI, VA |
| Device | CLASS II | Pinpoint Endoscopic Fluorescence Imaging System recalled | Novadaq Technologies | Sterility | Nationwide |
| Device | CLASS III | Non-sterile drape recalled by Novadaq Technologies | Novadaq Technologies | Labeling Errors | Nationwide |
| Device | CLASS III | LUNA Chest recalled by Novadaq Technologies | Novadaq Technologies | Labeling Errors | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.