Diversatek Healthcare recalls
Diversatek Healthcare has 7 recalls on record with the FDA and USDA, the earliest in 2022 and the latest reported on 29 Apr 2026. 6 are still ongoing. 4 were reported in the last 12 months.
Total recalls7since 2022
Last 12 months4reported
Class I00% of total
Ongoing6latest 29 Apr 2026
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 diversatek healthcare is recalled
Product types
By year
Ongoing diversatek healthcare recalls
6 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Viper¿ 3-Stage Fixed Wire Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS III | Zvu Anorectal Manometry Procedure Kit recalled by Diversatek Healthcare | Diversatek Healthcare | Labeling Errors | Nationwide |
| Device | CLASS III | ZVU Functional GI recalled by Diversatek Healthcare | Diversatek Healthcare | Labeling Errors | Nationwide |
All diversatek healthcare recalls, newest first
7 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Viper¿ 3-Stage Fixed Wire Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS III | Zvu Anorectal Manometry Procedure Kit recalled by Diversatek Healthcare | Diversatek Healthcare | Labeling Errors | Nationwide |
| Device | CLASS III | ZVU Functional GI recalled by Diversatek Healthcare | Diversatek Healthcare | Labeling Errors | Nationwide |
| Device | CLASS II | Diversatek Health, M-Catch Retrieval Nets recalled | Diversatek Healthcare | Packaging Defects | 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.