FDA Device recall Z-1970-2019
ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution
- FDA Device
- Class II
- terminated
- Published 2019-07-24
On 2019-07-24 the FDA classified a Class II recall of ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution by Pharmaceutical Innovations, citing potential for failed stability antimicrobial effectiveness testing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1970-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-06-19 |
| Published | 2019-07-24 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Pharmaceutical Innovations |
| Distribution | US |
Product
ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution.
Reason
Potential for failed stability antimicrobial effectiveness testing.
Identifiers
| code_info | Lot # 051914-60, 101615-60, 021317-60 |
|---|
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-1970-2019%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.