Berchtold recalls
Berchtold has 5 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 15 Jun 2016.
Total recalls5since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 15 Jun 2016
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 4 80%Class III 1 20%
Why berchtold is recalled
Product types
By year
All berchtold recalls, newest first
5 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Surgical Table Cushion (HybriGel Pads) HybrGel Pads are recalled | Berchtold | Other | Nationwide |
| Device | CLASS II | Teletom Equipment Management System recalled by Berchtold | Berchtold | Other | Nationwide |
| Device | CLASS II | Operon D850 Surgical Table recalled by Berchtold | Berchtold | Other | Nationwide |
| Device | CLASS II | Hand Controls for Operon D750, D752, D760, D820 recalled by Berchtold | Berchtold | Other | Nationwide |
| Device | CLASS III | Chromovision High Definition (HD) Wireless Camera, Pt # CC recalled | Berchtold | Device Malfunction | 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.