Class II — Parker Laboratories, Inc.
| Recalling firm | PARKER LABORATORIES, INC. |
|---|---|
| Registered facility | PARKER LABORATORIES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Product demonstrates low viscosity. |
| Product | Redux Electrolyte Creme, Product Ref. 66-04. Highly conductive electrolyte creme. |
| Quantity | 217 cases (1,085 Inner Boxes; 10,850 Eaches) |
| Distribution | Worldwide distribution - US Nationwide in the states of CA, CO, FL, GA, IL, MD, MI, MN, NC, NE, NY, OH, PA, SC, & TX. The countries of AU, CA, OM, & SA. |
| Initiated | 2024-03-22 |
| Classified | 2024-04-19 |
| Recall number | Z-1604-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Parker Laboratories, Inc. (Z-1604-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94303/
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