Beaver-Visitec International recalls
Beaver-Visitec International has 194 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 7 Jan 2026. 181 are still ongoing. 1 was reported in the last 12 months.
Total recalls194since 2014
Last 12 months1reported
Class I00% of total
Ongoing181latest 7 Jan 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 194 100%Class III 0 0%
Why beaver-visitec international is recalled
Product types
By year
Ongoing beaver-visitec international recalls
181 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | BVI Leos Laser and Endoscopy System recalled | Beaver-Visitec International | Manufacturing (CGMP) Deviations | Nationwide |
| Device | CLASS II | BVI CustomEyes Procedure Packs recalled by Beaver Visitec International | Beaver Visitec International | Other | Nationwide |
| Device | CLASS II | BVI CustomEyes Procedure Packs recalled by Beaver Visitec International | Beaver Visitec International | Other | Nationwide |
| Device | CLASS II | BVI CustomEyes Procedure Packs recalled by Beaver Visitec International | Beaver Visitec International | Other | Nationwide |
| Device | CLASS II | BVI CustomEyes Procedure Packs recalled by Beaver Visitec International | Beaver Visitec International | Other | Nationwide |
| Device | CLASS II | BVI CustomEyes Procedure Packs recalled by Beaver Visitec International | Beaver Visitec International | Other | Nationwide |
All beaver-visitec international recalls, newest first
194 totalAbout 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.