Richard Wolf recalls
Richard Wolf has 10 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 21 May 2025. 7 are still ongoing.
Total recalls10since 2018
Last 12 months0reported
Class I00% of total
Ongoing7latest 21 May 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 10 100%Class III 0 0%
Why richard wolf is recalled
Product types
By year
Ongoing richard wolf recalls
7 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | PiezoWave 2 Control Unit, Product Number 100506US recalled | Richard Wolf | Device Malfunction | GA |
| Device | CLASS II | Flex. Grasp. Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Flex. Grasp. Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Flex. Grasp. Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Flex. Biopsy Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Bronchoscope Tubes recalled by Richard Wolf | Richard Wolf | Sterility | Nationwide |
All richard wolf recalls, newest first
10 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | PiezoWave 2 Control Unit, Product Number 100506US recalled | Richard Wolf | Device Malfunction | GA |
| Device | CLASS II | Flex. Grasp. Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Flex. Grasp. Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Flex. Grasp. Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Flex. Biopsy Forceps WL, Product Number recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Cutting Electrode Bipo recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Tube Set for TEM recalled by Richard Wolf | Richard Wolf | Other | Nationwide |
| Device | CLASS II | Bronchoscope Tubes recalled by Richard Wolf | Richard Wolf | Sterility | Nationwide |
| Device | CLASS II | Artholine Punch B 4 H 1, used recalled by Richard Wolf | Richard Wolf | Other | |
| Device | CLASS II | Tube Set For Tem recalled by Richard Wolf | Richard Wolf | Other |
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.