Vygon MFG, Inc recalls
Vygon MFG, Inc has 9 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 4 Dec 2019. The most frequent reason is sterility.
Total recalls9since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 4 Dec 2019
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 9 100%Class III 0 0%
Why vygon mfg, inc is recalled
Product types
By year
All vygon mfg, inc recalls, newest first
9 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Single Lumen CT Midline Basic Tray, Product recalled by Vygon MFG, Inc | Vygon MFG, Inc | Other | TN |
| Device | CLASS II | Vygon IV Start Convenience Kits recalled by Vygon MFG, Inc | Vygon MFG, Inc | Potency & Assay | NH |
| Device | CLASS II | x .75 LifeGuard Huber Needle with Y-site recalled by Vygon MFG, Inc | Vygon MFG, Inc | Sterility | NH |
| Device | CLASS II | Nutrisafe 2 Syringe for Safety Connection recalled by Vygon MFG, Inc | Vygon MFG, Inc | Sterility | NH |
| Device | CLASS II | CVC Tray Pediatrics recalled by Vygon MFG, Inc | Vygon MFG, Inc | Sterility | NH |
| Device | CLASS II | Huber Needle Set recalled by Vygon MFG, Inc | Vygon MFG, Inc | Sterility | NH |
| Device | CLASS II | 3-Way Standardbore Stopcock recalled by Vygon MFG, Inc | Vygon MFG, Inc | Sterility | NH |
| Device | CLASS II | AMS-636, 60" Microbore extension set recalled by Vygon MFG, Inc | Vygon MFG, Inc | Packaging Defects | Nationwide |
| Device | CLASS II | AMS-651, 120" Microbore extension set with slide clamp recalled | Vygon MFG, Inc | Packaging Defects | CA |
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.