FDA Device recall Z-1604-2024
Redux Electrolyte Creme, Product Ref. 66-04
- FDA Device
- Class II
- ongoing
- Published 2024-05-01
On 2024-05-01 the FDA classified a Class II recall of Redux Electrolyte Creme, Product Ref. 66-04 by Parker Laboratories, citing product demonstrates low viscosity.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1604-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-22 |
| Published | 2024-05-01 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Parker Laboratories |
| Distribution | US |
Product
Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme.
Reason
Product demonstrates low viscosity.
Identifiers
| code_info | Product No. 66-04; UDI: 20855683006399 (Master), 10855683006392 (Inner Box), 00855683006395 (Each); Lot No. (Expiration…Product No. 66-04; UDI: 20855683006399 (Master), 10855683006392 (Inner Box), 00855683006395 (Each); Lot No. (Expiration Date): A1122010 (11/29/25) and A0523002 (5/12/26). |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1604-2024%22
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