FDA Device recall Z-0704-2020
HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03
- FDA Device
- Class II
- terminated
- Published 2019-12-25
On 2019-12-25 the FDA classified a Class II recall of HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03 by Bio Signal Group, citing product has the potential to be contaminated with Burkholderia cepacia (B. cepacia).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0704-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-10-29 |
| Published | 2019-12-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Bio Signal Group |
| Distribution | US |
Product
HydroDot brand: Wave Prep 4 oz. tubes-Product 1710-03. An electroconductive cream for use with external electrodes - Product Usage: An electroconductive cream for use with external electrodes to reduce the impedance of the contact between the electrode surface and the skin. The cream is not intended for use with stimulating electrodes.
Reason
Product has the potential to be contaminated with Burkholderia cepacia (B. cepacia)
Identifiers
| code_info | Product 1710-03: Lot # 29688 Expanded: Lot # 31160 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0704-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.