Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 21156 |
| Brand Name: | ConMed Electrosurgical Generators Monopolar/Bipolar |
| Model: | |
| Affected: | CONMED Hyfrecator® 2000 Electrosurgical Unit: Serial numbers 16020018, 16020032, 16020037, 16110158, 16160253, 16170278, 16170292, 16350421, 16380485, 16470584 |
| Software version: | |
| Recalling Organisation: | Paragon Care Group New Zealand Limited 69 Elizabeth Knox Place Glen Innes AUCKLAND |
| Contact Information: | 0508 654 258 |
| Manufacturer: | |
| Issue: | The Accessory Package contained within the Hyfrecator 2000 carton was packaged in error by the manufacturer,with non-sterile REF 7-796-19 Handpiece Sheaths in pouches that were labelled sterile. This could cause an end user to use a non-sterile sheath as if it were sterile. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 27/2/2017 |
